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X   Prescription Drugs: Alternative Uses, Alternative Cures: Over 1,500 New Uses for FDA-Approved Drugs How do I know if my medication is FDA approved? The agency is required to update the list quarterly. Good questions! Drug information typically includes the drug name, approval status, indication of use, and clinical trial results. This page lists cancer drugs approved by the Food and Drug Administration (FDA) for breast cancer. B   FDA approved 10 additional kits (4 PCR, 6 RAPID) as of 22 April 2020. B. marked it as to-read Dec 14, 2010. 9+3 (ASCORBIC ACID; BIOTIN; CYANOCOBALAMIN; DEXPANTHENOL; ERGOCALCIFEROL; FOLIC ACID; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN 5'-PHOSPHATE SODIUM; THIAMINE HYDROCHLORIDE; VITAMIN A; VITAMIN E), M.V.I. Note: If you need help accessing information in different file formats, see Instructions for Downloading Viewers and Players. Many unapproved drugs are marketed without brand names and have been available for many years, causing people to often assume that these unapproved drugs are generic drugs; however, this is not correct. a-methapred. You can keep taking these drugs as long as you are benefiting from treatment and not having … Despite so called protection for the consumer it appears that the FDA is nothing but a Monopoly enforcer, protecting drug companies. Language Assistance Available: Español | 繁體中文 | Tiếng Việt | 한국어 | Tagalog | Русский | العربية | Kreyòl Ayisyen | Français | Polski | Português | Italiano | Deutsch | 日本語 | فارسی | English, U.S. Department of Health and Human Services, M-ZOLE 3 COMBINATION PACK (MICONAZOLE NITRATE), M.V.C. The agency permits some unapproved drugs to be marketed if they are relied on by health care professionals to treat serious medical c… Its primary use is pain relief and it is administered in tablet form. Subsection 505(t)(3) defines an “authorized generic drug” as a listed drug as defined in § 314.3 that has been approved under subsection 505(c) of the act and is marketed, sold, or distributed directly or indirectly to retail class of trade with either labeling, packaging (other than repackaging as the listed drug in blister packs, unit doses, or similar packaging for use in institutions), product code, labeler code, trade name, or trade mark that differs from that of the listed drug. Lack of approval reminds consumers that a product has not received the same rigorous testing as approved drugs and … ibandronate sodium (ibandronate sodium) | anda #078995 | tablet;oral | mylan pharms inc ibandronate sodium (ibandronate sodium) | anda #078996 | tablet;oral | sun pharm industries ibandronate sodium (ibandronate sodium) | anda #078997 | tablet;oral | dr reddys labs ltd ibandronate sodium (ibandronate sodium) | anda #078998 | tablet;oral | orchid … P   Data sources include IBM Watson Micromedex (updated 2 Feb 2021), Cerner Multum™ (updated 3 Feb … There are common prescription drugs which we’ve mentioned in this article, in addition to a number of over-the-counter supplements. Data sources include IBM Watson Micromedex (updated 2 Feb 2021), Cerner Multum™ (updated 3 Feb … A generic drug is the same as the brand-name drug in active ingredient, conditions of use, dosage form, strength, route of administration, and (with certain permissible differences) labeling. No. Write a review. R   UPDATE (October 14, 2019): Recently approved by the U.S. Food and Drug Administration for the treatment of Parkinson's “off” time – when symptoms reemerge between doses – Nourianz (istradefylline) now is available by prescription. Other than the fact that it does not have the brand name on its label, it is the exact same drug product as the branded product. Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. The NDA holder may market both the authorized generic and the brand-name product at the same time. ADULT (PHARMACY BULK PACKAGE) (ASCORBIC ACID; BIOTIN; CYANOCOBALAMIN; DEXPANTHENOL; ERGOCALCIFEROL; FOLIC ACID; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN 5'-PHOSPHATE SODIUM; THIAMINE HYDROCHLORIDE; VITAMIN A; VITAMIN E; VITAMIN K), M.V.I. Data sources include IBM Watson Micromedex (updated 2 Feb 2021), Cerner Multum™ (updated 3 Feb … Abbreviated New Drug Application (ANDA): 211081 Company: APOLLO . People assume that all prescribed medicines are safe, but not following instructions or combining them with other medicines, drugs and/or alcohol can be dangerous. This page also lists common drug combinations used in breast cancer. Human drugs have medication warnings but animal owners don't get prescription inserts and in 2019 vets still don't warn of side effects or deadly adverse reactions. D   The drug industry has taken nature, patented it and fleeced us with the collaboration of governments the World over. For approval of a generic drug, the FDA requires scientific evidence that the generic drug is interchangeable with or therapeutically equivalent to the originally approved drug. We went on a mission to find the most dangerous FDA approved money could buy, their side effects and possible natural remedies. FDA Approves Gemtesa (vibegron) Tablets for the Treatment of Patients with Overactive Bladder (OAB) - December 23, 2020 medical air, usp (medical air) | nda #205890 | gas;inhalation | matheson tri-gas inc medical air, usp (medical air) | nda #207036 | gas;inhalation | cee kay supply medical air, usp (medical air) | nda #207114 | gas;inhalation | american welding and gas inc medical air, usp (medical air) | nda #205711 | gas;inhalation | air liquide america speciality gases L   Company; COZAAR: LOSARTAN POTASSIUM: 100MG: TABLET;ORAL: Prescription A   Anabolic medication builds new bone, increases bone density, and lowers the risk of broken bones. The drug, named lemborexant (Dayvigo), was … The source of FDALabel's data is the FDA's Structured Product Labeling (SPL)1 archive2,3, which stores labeling documents submitted by manufacturers. An authorized generic is considered to be therapeutically equivalent to its brand-name drug because it is the same drug. These quantities are based on recognized standards of care as well as from FDA-approved dosing guidelines. The FDA in 2010 approved another prescription-only app, called BlueStar, for use by people with Type 2 diabetes. The cannabinoid research is focusing on a drug currently titled WIN55, similar to THC but with a different chemical structure and HU-210, a more potent synthetic to THC with extended duration of action. Z   Therefore, it is generally less costly to obtain approval of a generic drug than a brand name drug. Share; Tweet; Linkedin; Pin it; More sharing options. Cholinesterase inhibitors are prescribed to treat symptoms related to memory, thinking, language, judgment and other thought processes. Generic drugs must be proven bioequivalent (that they work the same) as the brand name medication. FDA approved weight loss supplements represent a safe choice when it comes to weight management. A-Z list of drugs, Learn about Acamprosate, Actiq, Adderall, Alcohol, Alprazolam, Ambien, ... Adderall has known abuse liability and should be used in accordance with a prescription from a medical professional. The drugs are listed alphabetically. This list is not limited to drugs that were ever approved by the FDA. A wide variety of medications exist that lead to … a-methapred (methylprednisolone sodium succinate) | anda #089573 | injectable;injection | abbott a-methapred (methylprednisolone sodium succinate) | anda #089574 | injectable;injection | abbott a-methapred (methylprednisolone sodium succinate) | anda #089575 | injectable;injection | abbott a-methapred (methylprednisolone sodium succinate) | anda … BlueStar offers motivational and educational messages, and … This material is provided for educational purposes only and is not intended for medical advice, diagnosis or treatment. Action Date Submission Action Type Submission Classification Review Priority; … Gemtesa (vibegron) is a once-daily beta-3 adrenergic agonist indicated for the treatment of overactive bladder (OAB) with symptoms of urge urinary incontinence, urgency, and urinary frequency in adults. Obesity is considered a chronic (long-term) disease, similar to high blood pressure or diabetes. ... Over 1,500 New Uses for FDA-Approved Drugs. Drugs.com provides accurate and independent information on more than 24,000 prescription drugs, over-the-counter medicines and natural products. N   What’s the meaning of this? Where risks or harms is the reason for withdrawal, this will usually have been prompted by unexpected adverse effects that were not detected during Phase III clinical trials, i.e. FDA regulates the safety and effectiveness of prescription and over-the-counter (OTC) drugs, and works to help communicate the benefits and risks associated with these products. Below are the 35 drugs we could find that have been recalled from the US market since the 1970s, some that had been in use since the 1930s. This material is provided for educational purposes only and is not intended for medical advice, diagnosis or treatment. H   FDA publishes a list of reported authorized generics and updates that list quarterly. In some cases, even though it is the same as the brand name product, a company may choose to sell the authorized generic at a lower cost than the brand name drug. All of the prescription medications currently approved to treat Alzheimer's symptoms in early to moderate stages are from a class of drugs called cholinesterase inhibitors. Antiresorptive medication prevents bone loss, may increase bone density, and lowers the risk of broken bones. Did you know? Drug-related deaths from prescribed drugs … Antiresorptive medications include a class of drugs called bisphosphonates. Read more about Nourinanz and other Parkinson’s … These drugs are approved to treat erectile dysfunction (ED). From abbreviated new drug application to therapeutic equivalence codes, FDA defines it. As of 2012, 80% of all FDA approved drugs are available in generic form. Among other things, FDAAA added new subsection (t) to section 505 of the Federal Food, Drug, and Cosmetic Act (the Act). Section 505(t) is titled “Database For Authorized Generic Drugs,” and requires that FDA publish a complete list on its Internet site of all authorized generic drugs, including (1) the drug trade name, (2) the brand company manufacturer, and (3) the date the authorized generic drug entered the market. Drugs are placed on the list by a committee of local doctors, pharmacists and Priority Health staff who review current research to determine which drugs are the most effective. You may e-mail questions about the List of Authorized Generics Drugs to:AuthorizedGenerics@fda.hhs.gov, An official website of the United States government, : Section deals with the comprehensive list of drugs approved by FDA in 2014. Prescription drugs. C   K   Only one of these drugs, called tadalifil (Cialis), is also FDA-approved to help relieve BPH symptoms. See Medicines and Healthcare products Regulatory Agency. Here's what you need to know. As a result of this posture, FDA approval usually signals that a new product is safe and reliable. In some cases, you may even get generic medications for free. This material is provided for educational purposes only and is not intended for medical advice, diagnosis or treatment. The Approved Drug List, sometimes called a formulary, is a list of drugs your plan includes. Barbara J. Andrews, Journalist, AKC Master Breeder. Some prescription drugs that are not FDA approved, and not otherwise excluded, will be covered under the prescription drug benefit for certain plans as required by the Patient Protection and Affordable Care Act (PPACA) or as defined in the member’s benefit booklet These items include but may not be limited Read reviews from world’s largest community for readers. While a separate NDA is not required for marketing an authorized generic, FDA requires that the NDA holder notify the FDA if it markets an authorized generic. Of course, diet and exercise should always be the way to go. T   Medicines prescribed by a doctor — also known as pharmaceuticals — that are not being used appropriately can cause harm, both short and long-term. Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url; 11/02/2020: SUPPL-18: Labeling-Package Insert The following table lists th… As part of their required annual reports, NDA holders must notify the FDA of any authorized generic drugs marketed under their approved NDAs. some prescription drugs. The agency balances its goal to eliminate unapproved prescription drugs from the market with patient access to medically necessary drugs. ; As such, it usually requires long-term treatment to successfully lose weight and keep it off. For over 100 years, the U.S. Food and Drug Administration (FDA) has defined itself through reliance on scientific evidence over political rhetoric. Additionally, cholinesterase inhibitors: Prevent the breakdown of … Y   This page lists selected prescription drugs that have NOT BEEN APPROVED by the FDA. U   In addition, an authorized generic version of a tablet or capsule may have a different color or marking. October 16, 2019. To obtain approval of a generic drug, a company must submit an Abbreviated New Drug Application (ANDA) to FDA and prove that its product is the same as the brand-name drug in the ways described above, and that it is “bioequivalent,” meaning it gets to the part of the body where the drug works at the same time and in the same amount. The table below lists FDA-approved prescription medications for weight loss. Domperidone is not FDA approved in the United States for any indication. Data sources include IBM Watson Micromedex (updated 2 Feb 2021), Cerner Multum™ (updated 3 Feb … lack of demand and relatively high production costs). FDALabel Database is a web-based application that allows users to perform customizable searches of a database containing over 100,000 drug labeling documents for FDA-approved drug … These act like coupons and allow you to bypass insurance altogether. Epidiolex, the first FDA-approved medication made from marijuana, is now available by prescription in the United States. We're going to see a lot more consumer tech devices get the FDA's blessing. The drug-approval process is complicated—and it has a complicated history. Lack of approval reminds consumers that a product has not received the same rigorous testing as approved drugs and … Prescription Drugs book. Some are also used for OAB with urge urinary incontinence (UUI). However, the drug combinations themselves usually are not approved, although they are widely … Opioids top the list of most commonly abused prescription drugs, even being high on the list of most commonly abused drugs of all kinds. Our Best FDA Approved Appetite Suppressant Conclusion. The list includes generic and brand names. The FDA approved medications, or drugs, currently available on the U.S. market for the treatment of urinary incontinence are for a specific condition called overactive bladder (OAB). An authorized generic may be marketed by the brand name drug company, or another company with the brand company’s permission. Max Macaluso. For over 100 years, the U.S. Food and Drug Administration (FDA) has defined itself through reliance on scientific evidence over political rhetoric. That means no deductibles. The individual drugs in the combinations are FDA-approved. Welcome to the Drugs@FDA glossary of terms. V   She was asked to refill a prescription for a drug called domperidone to help a patient with lactation. What are the FDA-approved medications for osteoporosis? Tramadol is a prescription painkiller somewhat unique amongst other opioid agonist drugs due to its serotonin and norepinephrine reuptake inhibiting properties. The FDA has REFUSED to provide a list of unapproved drugs, … Medication Guides are paper handouts that come with many prescription medicines. Their paper, "An Overview of FDA-Approved New Molecular Entities (NMEs): 1827-2013," is an ambitious attempt to tally up all products approved by FDA and its numerous predecessor agencies since its inception. Abbreviated New Drug Application (ANDA), Recalls, Market Withdrawals and Safety Alerts, Generic Drugs Program Activities Report - Monthly Performance, Abbreviated New Drug Application (ANDA) Forms and Submission Requirements, Patent Certifications and Suitability Petitions, Approved Drug Products With Therapeutic Equivalence Evaluations, Food and Drug Administration Amendments Act (FDAAA) (Public Law 110-85). This material is provided for educational purposes only and is not intended for medical advice, diagnosis or treatment. FDA carefully considers the possible effects on patient access, including whether any action would likely lead to a disruption in the drug supply, before initiating an action against an unapproved drug. The CDC reports that three out of four people who initiate heroin use began by abusing a prescription opioid, close to half of those who use heroin are addicted to prescription opioids, and nine out of 10 also abuse another drug. Antiresorptive medications include a class of drugs called bisphosphonates. Products listed on this page may not be equivalent to one another. However, a generic drug may have certain minor differences from the brand-name product, such as different inactive ingredients. Before sharing sensitive information, make sure you're on a federal government site. The Orphan Drug Act was passed in 1983 to give drug companies incentives to develop treatments for rare diseases. What are the FDA-approved medications for osteoporosis? Section 505(t)(2) of the Act requires the list to contain authorized generic drugs included in an annual report submitted to the agency after January 1, 1999. 3 prescription drugs that come from marijuana. ibandronate sodium. Note that the prescription medications FDA-approved for the treatment of insomnia (listed below) include (in no particular order): Benzodiazepines (estazolam, flurazepam, quazepam, temazepam, triazolam) The so-called “Z drugs” (eszopiclone, zaleplon, zolpidem) A tricyclic antidepressant (doxepin) Many manufacturers also introduced drugs onto the market between 1938 and 1962 based on: – Their own conclusion that the products were GRAS (i.e., not a “new … As of 2012, 80% of all FDA approved drugs are available in generic form. S   As a result of this posture, FDA approval usually signals that a new product is safe and reliable. The FDALabel Database is a web-based application used to perform customizable searches of over 110,000 human prescription, biological, over-the-counter (OTC), and animal drug labeling documents. But that's not the whole story. On September 27, 2007, the President signed into law the Food and Drug Administration Amendments Act (FDAAA) (Public Law 110-85). The FDA List of Authorized Generics page answers what an authorized generic is and how it differs from a traditional generic. FDA APPROVED VETERINARY DRUGS. In 1989, a major scandal erupted involving the procedures used by the FDA to approve generic drugs … These medications include: … Drugs.com provides accurate and independent information on more than 24,000 prescription drugs, over-the-counter medicines and natural products. Other product names: Linkedin; Pin it; Email; Print; Home | Previous Page. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. Company; FEBUXOSTAT: FEBUXOSTAT: 40MG: TABLET;ORAL: Prescription Q   List of drugs used to treat the medical condition called Hypoxemia. An authorized generic is … A generic drug, as that term is commonly understood and referred to by health care providers and insurers, is a copy of a brand-name drug that is developed and made by a company other than the company that makes the brand-name drug. FDALabel is implemented as a secure three-tier platform with an Oracle database. I   FDA Approved Drugs The following database contains a listing of drugs approved by the Food and Drug Administration (FDA) for sale in the United States. Hard to believe but this system has been in decades in the making. W   An ANDA applicant is not required to provide independent evidence of the safety and effectiveness of a proposed generic drug. This is called an Abbreviated New Drug Application (ANDA). You may have seen advertisements on television or in magazines for these medications. Anabolic medication builds new bone, increases bone density, and lowers the risk of broken bones. For purposes of this policy, a U.S. Food and Drug Administration (FDA)-approved prescription drug is defined as an FDA-approved drug, biological, or compounded prescription which, by State and Federal Law, may be dispensed only by prescription or administered by a person who is acting within his or her capacity as a paid health professional. The Center for Drug Evaluation and Research (CDER) ensures that safe and effective drugs are available to improve the health of the people in the United States * Drugs@FDA includes information about drugs, including biological products, approved for human use in the United States (see FAQ), but does not include information about FDA-approved products regulated by the Center for Biologics Evaluation and Research (for example, vaccines, allergenic products, blood and blood products, plasma derivatives, cellular and gene therapy … J   FDA approved vs. FDA cleared: Why you need to know the difference. Drugs.com provides accurate and independent information on more than 24,000 prescription drugs, over-the-counter medicines and natural products. Nur Izzati marked it as to-read Dec 08, 2012. It does not include medicinal ingredients that when found in a drug, require a prescription if those ingredients are listed in Controlled Drugs and Substances Act Schedules. Drug information includes the drug name and indication of use. PEDIATRIC (ASCORBIC ACID; BIOTIN; CYANOCOBALAMIN; DEXPANTHENOL; ERGOCALCIFEROL; FOLIC ACID; NIACINAMIDE; PHYTONADIONE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN 5'-PHOSPHATE SODIUM; THIAMINE HYDROCHLORIDE; VITAMIN A; VITAMIN E), M.V.I.-12 ADULT (ASCORBIC ACID; BIOTIN; CYANOCOBALAMIN; DEXPANTHENOL; ERGOCALCIFEROL; FOLIC ACID; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN 5'-PHOSPHATE SODIUM; THIAMINE HYDROCHLORIDE; VITAMIN A; VITAMIN E), M.V.I.-12 LYOPHILIZED (ASCORBIC ACID; BIOTIN; CYANOCOBALAMIN; DEXPANTHENOL; ERGOCALCIFEROL; FOLIC ACID; NIACINAMIDE; PYRIDOXINE; RIBOFLAVIN 5'-PHOSPHATE SODIUM; THIAMINE; VITAMIN A; VITAMIN E), MACROBID (NITROFURANTOIN; NITROFURANTOIN, MACROCRYSTALLINE), MACRODANTIN (NITROFURANTOIN, MACROCRYSTALLINE), MACROTEC (TECHNETIUM TC-99M ALBUMIN AGGREGATED KIT), MAGNESIUM HYDROXIDE AND OMEPRAZOLE AND SODIUM BICARBONATE, MAGNESIUM HYDROXIDE AND OMEPRAZOLE AND SODIUM BICARBONATE (MAGNESIUM HYDROXIDE; OMEPRAZOLE; SODIUM BICARBONATE), MAGNESIUM SULFATE ANHYDROUS; POTASSIUM SULFATE; SODIUM SULFATE, MAGNESIUM SULFATE ANHYDROUS; POTASSIUM SULFATE; SODIUM SULFATE (MAGNESIUM SULFATE ANHYDROUS; POTASSIUM SULFATE; SODIUM SULFATE), MAGNESIUM SULFATE IN DEXTROSE 5% IN PLASTIC CONTAINER, MAGNESIUM SULFATE IN DEXTROSE 5% IN PLASTIC CONTAINER (MAGNESIUM SULFATE), MAGNESIUM SULFATE IN PLASTIC CONTAINER (MAGNESIUM SULFATE), MAKENA (AUTOINJECTOR) (HYDROXYPROGESTERONE CAPROATE), MAKENA PRESERVATIVE FREE (HYDROXYPROGESTERONE CAPROATE), MALARONE (ATOVAQUONE; PROGUANIL HYDROCHLORIDE), MALARONE PEDIATRIC (ATOVAQUONE; PROGUANIL HYDROCHLORIDE), MALMOREDE (ETHINYL ESTRADIOL; ETHYNODIOL DIACETATE), MANGANESE CHLORIDE IN PLASTIC CONTAINER (MANGANESE CHLORIDE), MANNITOL 10% IN PLASTIC CONTAINER (MANNITOL), MANNITOL 10% W/ DEXTROSE 5% IN DISTILLED WATER, MANNITOL 10% W/ DEXTROSE 5% IN DISTILLED WATER (MANNITOL), MANNITOL 15% IN PLASTIC CONTAINER (MANNITOL), MANNITOL 15% W/ DEXTROSE 5% IN SODIUM CHLORIDE 0.45%, MANNITOL 15% W/ DEXTROSE 5% IN SODIUM CHLORIDE 0.45% (MANNITOL), MANNITOL 20% IN PLASTIC CONTAINER (MANNITOL), MANNITOL 5% IN PLASTIC CONTAINER (MANNITOL), MANNITOL 5% W/ DEXTROSE 5% IN SODIUM CHLORIDE 0.12%, MANNITOL 5% W/ DEXTROSE 5% IN SODIUM CHLORIDE 0.12% (MANNITOL), MAPROTILINE HYDROCHLORIDE (MAPROTILINE HYDROCHLORIDE), MARCAINE HYDROCHLORIDE (BUPIVACAINE HYDROCHLORIDE), MARCAINE HYDROCHLORIDE PRESERVATIVE FREE (BUPIVACAINE HYDROCHLORIDE), MARCAINE HYDROCHLORIDE W/ EPINEPHRINE (BUPIVACAINE HYDROCHLORIDE; EPINEPHRINE BITARTRATE), MARCAINE HYDROCHLORIDE W/ EPINEPHRINE PRESERVATIVE FREE, MARCAINE HYDROCHLORIDE W/ EPINEPHRINE PRESERVATIVE FREE (BUPIVACAINE HYDROCHLORIDE; EPINEPHRINE BITARTRATE), MARLISSA (ETHINYL ESTRADIOL; LEVONORGESTREL), MAXITROL (DEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE), MAXZIDE (HYDROCHLOROTHIAZIDE; TRIAMTERENE), MAXZIDE-25 (HYDROCHLOROTHIAZIDE; TRIAMTERENE), MD-60 (DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM), MD-76 (DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM), MD-76R (DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM), MD-GASTROVIEW (DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM), MDP-BRACCO (TECHNETIUM TC-99M MEDRONATE KIT), MECAMYLAMINE HYDROCHLORIDE (MECAMYLAMINE HYDROCHLORIDE), MECLIZINE HYDROCHLORIDE (MECLIZINE HYDROCHLORIDE), MECLOFENAMATE SODIUM (MECLOFENAMATE SODIUM), MEDIGESIC PLUS (ACETAMINOPHEN; BUTALBITAL; CAFFEINE), MEDIHALER ERGOTAMINE (ERGOTAMINE TARTRATE), MEDROL ACETATE (METHYLPREDNISOLONE ACETATE), MEDROXYPROGESTERONE ACETATE (MEDROXYPROGESTERONE ACETATE), MEFLOQUINE HYDROCHLORIDE (MEFLOQUINE HYDROCHLORIDE), MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER, MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER (CEFOXITIN SODIUM), MEFOXIN IN PLASTIC CONTAINER (CEFOXITIN SODIUM), MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER, MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER (CEFOXITIN SODIUM), MELAMISA (DROSPIRENONE; ETHINYL ESTRADIOL), MELPHALAN HYDROCHLORIDE (MELPHALAN HYDROCHLORIDE), MEMANTINE HYDROCHLORIDE (MEMANTINE HYDROCHLORIDE), MEMANTINE HYDROCHLORIDE AND DONEPEZIL HYDROCHLORIDE, MEMANTINE HYDROCHLORIDE AND DONEPEZIL HYDROCHLORIDE (DONEPEZIL HYDROCHLORIDE; MEMANTINE HYDROCHLORIDE), MENRIUM 10-4 (CHLORDIAZEPOXIDE; ESTROGENS, ESTERIFIED), MENRIUM 5-2 (CHLORDIAZEPOXIDE; ESTROGENS, ESTERIFIED), MENRIUM 5-4 (CHLORDIAZEPOXIDE; ESTROGENS, ESTERIFIED), MEPERGAN (MEPERIDINE HYDROCHLORIDE; PROMETHAZINE HYDROCHLORIDE), MEPERIDINE AND ATROPINE SULFATE (ATROPINE SULFATE; MEPERIDINE HYDROCHLORIDE), MEPERIDINE HYDROCHLORIDE (MEPERIDINE HYDROCHLORIDE), MEPERIDINE HYDROCHLORIDE PRESERVATIVE FREE, MEPERIDINE HYDROCHLORIDE PRESERVATIVE FREE (MEPERIDINE HYDROCHLORIDE), MEPIVACAINE HYDROCHLORIDE (MEPIVACAINE HYDROCHLORIDE), MEPIVACAINE HYDROCHLORIDE W/ LEVONORDEFRIN, MEPIVACAINE HYDROCHLORIDE W/ LEVONORDEFRIN (LEVONORDEFRIN; MEPIVACAINE HYDROCHLORIDE), MEPROBAMATE AND ASPIRIN (ASPIRIN; MEPROBAMATE), MERETEK UBT KIT (W/ PRANACTIN) (UREA C-13), MEROPENEM AND SODIUM CHLORIDE IN DUPLEX CONTAINER, MEROPENEM AND SODIUM CHLORIDE IN DUPLEX CONTAINER (MEROPENEM), MERSALYL-THEOPHYLLINE (MERSALYL SODIUM; THEOPHYLLINE), MERZEE (ETHINYL ESTRADIOL; NORETHINDRONE ACETATE), METADATE CD (METHYLPHENIDATE HYDROCHLORIDE), METADATE ER (METHYLPHENIDATE HYDROCHLORIDE), METAGLIP (GLIPIZIDE; METFORMIN HYDROCHLORIDE), METAPROTERENOL SULFATE (METAPROTERENOL SULFATE), METARAMINOL BITARTRATE (METARAMINOL BITARTRATE), METATENSIN #2 (RESERPINE; TRICHLORMETHIAZIDE), METATENSIN #4 (RESERPINE; TRICHLORMETHIAZIDE), METFORMIN HYDROCHLORIDE (METFORMIN HYDROCHLORIDE), METFORMIN HYDROCHLORIDE AND SITAGLIPTIN PHOSPHATE, METFORMIN HYDROCHLORIDE AND SITAGLIPTIN PHOSPHATE (METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE), METFORMIN HYDROCHLORIDE AND SITAGLIPTIN PHOSPHATE, METFORMIN HYDROCHLORIDE AND SITAGLIPTIN PHOSPHATE (METFORMIN HYDROCHLORIDE;SITAGLIPTIN PHOSPHATE ), METHADONE HYDROCHLORIDE (METHADONE HYDROCHLORIDE), METHADONE HYDROCHLORIDE INTENSOL (METHADONE HYDROCHLORIDE), METHAMPEX (METHAMPHETAMINE HYDROCHLORIDE), METHAMPHETAMINE HYDROCHLORIDE (METHAMPHETAMINE HYDROCHLORIDE), METHDILAZINE HYDROCHLORIDE (METHDILAZINE HYDROCHLORIDE), METHENAMINE HIPPURATE (METHENAMINE HIPPURATE), METHOCARBAMOL AND ASPIRIN (ASPIRIN; METHOCARBAMOL), METHOTREXATE PRESERVATIVE FREE (METHOTREXATE SODIUM), METHOTREXATE SODIUM (METHOTREXATE SODIUM), METHOTREXATE SODIUM (CALCIUM CHLORIDE; DEXTROSE; GLUTATHIONE DISULFIDE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM PHOSPHATE), METHOTREXATE SODIUM PRESERVATIVE FREE (METHOTREXATE SODIUM), METHSCOPOLAMINE BROMIDE (METHSCOPOLAMINE BROMIDE), METHYCLOTHIAZIDE AND DESERPIDINE (DESERPIDINE; METHYCLOTHIAZIDE), METHYLDOPA AND CHLOROTHIAZIDE (CHLOROTHIAZIDE; METHYLDOPA), METHYLDOPA AND HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE; METHYLDOPA), METHYLDOPATE HCL (METHYLDOPATE HYDROCHLORIDE), METHYLDOPATE HYDROCHLORIDE (METHYLDOPATE HYDROCHLORIDE), METHYLERGONOVINE MALEATE (METHYLERGONOVINE MALEATE), METHYLIN ER (METHYLPHENIDATE HYDROCHLORIDE), METHYLNALTREXONE BROMIDE (METHYLNALTREXONE BROMIDE), METHYLPHENIDATE HYDROCHLORIDE (METHYLPHENIDATE HYDROCHLORIDE), METHYLPREDNISOLONE (METHYLPREDNISOLONE SODIUM SUCCINATE), METHYLPREDNISOLONE ACETATE (METHYLPREDNISOLONE ACETATE), METHYLPREDNISOLONE SODIUM SUCCINATE (METHYLPREDNISOLONE SODIUM SUCCINATE), METIMYD (PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM), METIPRANOLOL (METIPRANOLOL HYDROCHLORIDE), METOCLOPRAMIDE (METOCLOPRAMIDE HYDROCHLORIDE), METOCLOPRAMIDE HCL (METOCLOPRAMIDE HYDROCHLORIDE), METOCLOPRAMIDE HYDROCHLORIDE (METOCLOPRAMIDE HYDROCHLORIDE), METOCLOPRAMIDE INTENSOL (METOCLOPRAMIDE HYDROCHLORIDE), METOPROLOL SUCCINATE (METOPROLOL SUCCINATE), METOPROLOL TARTRATE (METOPROLOL TARTRATE), METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE, METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE), METOZOLV ODT (METOCLOPRAMIDE HYDROCHLORIDE), METRO I.V. 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