Drug & Medication Database
Browse 18,617 FDA-approved medications with detailed information about uses, dosage, side effects, and interactions.
Metoclopramide Hydrochloride Monohydrate
metoclopramide hydrochloride monohydrate
Dosage form: POWDER. Active ingredients: METOCLOPRAMIDE HYDROCHLORIDE (1 kg/kg). Category: BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING.
Metocurine Iodide
metocurine iodide
Manufactured by QUAD PHARMS. Dosage form: Injectable. Route: Injection. Active ingredients: METOCURINE IODIDE (2MG/ML). Application: ANDA089443.
Metolazone
metolazone
DESCRIPTION Metolazone Tablets, USP for oral administration contain 2.5 mg, 5 mg or 10 mg of metolazone, USP, a diuretic/saluretic/antihypertensive drug of the quinazoline class. Metolazone has the molecular formula C 16 H 16 ClN 3 O 3 S, the chemical name 7-chloro-1, 2, 3, 4-tetrahydro-2-methyl-3-(2-methylphenyl)-4-oxo-6-quinazolinesulfonamide, and a molecular weight of 365.83.
Brands: Metolazone
Metopimazine
metopimazine
Dosage form: POWDER. Active ingredients: METOPIMAZINE (100 kg/100kg). Category: BULK INGREDIENT.
Metoprolol
metoprolol
11 DESCRIPTION Metoprolol tartrate tablets, USP contain metoprolol tartrate, USP a selective beta 1 -adrenoreceptor blocking agent. Metoprolol tartrate, USP is (±)-1-(Isopropylamino)-3-[p-(2-methoxyethyl) phenoxy]-2-propanol L-(+)tartrate (2:1) salt, and its structural formula is Metoprolol tartrate, USP is a white, practically odorless, crystalline powder with a molecular weight of 684.82.
Brands: Metoprolol Tartrate
Metoprolol Fumarate
metoprolol fumarate
Manufactured by NOVARTIS. Dosage form: TABLET, EXTENDED RELEASE. Route: ORAL. Active ingredients: METOPROLOL FUMARATE (EQ 200MG TARTRATE). Application: NDA019786.
Metoprolol Succinate
metoprolol succinate
11 DESCRIPTION TOPROL-XL, metoprolol succinate, is a beta 1 -selective (cardioselective) adrenoceptor blocking agent, for oral administration, available as extended-release tablets. TOPROL-XL has been formulated to provide a controlled and predictable release of metoprolol for once-daily administration. The tablets comprise a multiple unit system containing metoprolol succinate in a multitude of controlled release pellets.
Brands: Toprol Xl
Metoprolol Succinate Er
metoprolol succinate er
Metoprolol succinate, is a beta 1-selective (cardioselective) adrenoceptor blocking agent, for oral administration, available as extended-release tablets. Metoprolol succinate extended-release tablets has been formulated to provide a controlled and predictable release of metoprolol for once-daily administration. The tablets comprise a multiple unit system containing metoprolol succinate in a multitude of controlled release pellets.
Brands: Metoprolol Succinate Er
Metoprolol Succinate Er Tablets
metoprolol succinate er tablets
Metoprolol succinate ER tablets are a beta-1 selective adrenergic blocker in extended-release form indicated for treating hypertension, angina pectoris, and heart failure.
Brands: Metoprolol Succinate
Metoprolol Tartrate
metoprolol tartrate
11 DESCRIPTION Metoprolol tartrate tablets, USP contain metoprolol tartrate, a selective beta 1 -adrenoreceptor blocking agent. Metoprolol tartrate is (±)-1-(Isopropylamino)-3-[p-(2-methoxyethyl) phenoxy]-2-propanol L-(+)-tartrate (2:1) salt, and its structural formula is Metoprolol tartrate, USP is a white, crystalline powder with a molecular weight of 684.82.
Brands: Metoprolol Tartrate
Metoprolol Tartrate And Hydrochlorothiazide
metoprolol tartrate and hydrochlorothiazide
11 DESCRIPTION Metoprolol tartrate and hydrochlorothiazide tablets, USP has the antihypertensive effect of metoprolol tartrate, a beta adrenoreceptor blocker, and hydrochlorothiazide, a thiazide diruetic. It is available as tablets for oral administration. The 50/25 tablets contain 50 mg of metoprolol tartrate USP and 25 mg of hydrochlorothiazide USP and the 100/25 tablets contain 100 mg of metoprolol tartrate USP and 25 mg of hydrochlorothiazide USP.
Brands: Metoprolol Tartrate And Hydrochlorothiazide
Metoprolol Tartrate Ds/ip
metoprolol tartrate ds/ip
Dosage form: POWDER. Active ingredients: METOPROLOL TARTRATE (1 kg/kg). Category: BULK INGREDIENT.
Metoroprolol Tartrate
metoroprolol tartrate
11 DESCRIPTION Metoprolol Tartrate Injection, USP is a selective beta 1 -adrenoreceptor blocking agent, available in 5 mL and oversized 10 mL vials for intravenous administration. Each vial contains a sterile solution of Metoprolol Tartrate USP, 5 mg, and Sodium Chloride, USP, 45 mg, and Water for Injection, USP.
Brands: Metoprolol Tartrate
Metreleptin
metreleptin
11 DESCRIPTION MYALEPT (metreleptin) for injection is a recombinant human leptin analog for injection that binds to and activates the leptin receptor. Metreleptin (recombinant methionyl-human leptin) is produced in E. coli and differs from native human leptin by the addition of a methionine residue at its amino terminus. Metreleptin is a 147-amino acid, nonglycosylated, polypeptide with one disulfide bond between Cys-97 and Cys-147 and a molecular weight of approximately 16.15 kDa.
Brands: Myalept
Metrizamide
metrizamide
Manufactured by GE HEALTHCARE. Dosage form: INJECTABLE. Route: INJECTION. Active ingredients: METRIZAMIDE (3.75GM/VIAL). Application: NDA017982.
Metrizoate Magnesium
metrizoate magnesium
Manufactured by GE HEALTHCARE. Dosage form: INJECTABLE. Route: INJECTION. Active ingredients: CALCIUM METRIZOATE (0.78MG/ML); MEGLUMINE METRIZOATE (75.9MG/ML); METRIZOATE MAGNESIUM (0.15MG/ML); METRIZOATE SODIUM (16.6MG/ML). Application: NDA016847.
Metrizoate Sodium
metrizoate sodium
Manufactured by GE HEALTHCARE. Dosage form: INJECTABLE. Route: INJECTION. Active ingredients: CALCIUM METRIZOATE (0.78MG/ML); MEGLUMINE METRIZOATE (75.9MG/ML); METRIZOATE MAGNESIUM (0.15MG/ML); METRIZOATE SODIUM (16.6MG/ML). Application: NDA016847.
Metrizoic Acid
metrizoic acid
Manufactured by GE HEALTHCARE. Dosage form: INJECTABLE. Route: INJECTION. Active ingredients: CALCIUM (0.35MG/ML); MEGLUMINE (140.1MG/ML); METRIZOIC ACID (461.8MG/ML). Application: NDA017506.
Metronidazole
metronidazole
DESCRIPTION Metronidazole tablets, USP 250 mg or 500 mg is an oral formulation of the synthetic nitroimidazole antimicrobial, 2-methyl-5-nitro-1H-imidazole-1-ethanol, which has the following structural formula: Metronidazole tablets USP contain 250 mg or 500 mg of metronidazole. Inactive ingredients include powdered cellulose, hydroxypropyl cellulose, low substituted hydroxypropyl cellulose, hypromellose, polyethylene glycol, stearic acid, and titanium dioxide. Molecular Structure
Brands: Metronidazole
Metronidazole Benzoate
metronidazole benzoate
Dosage form: POWDER. Active ingredients: METRONIDAZOLE BENZOATE (1 kg/kg). Category: BULK INGREDIENT.
Metronidazole Benzoate Micronized
metronidazole benzoate micronized
Dosage form: POWDER. Active ingredients: METRONIDAZOLE (1 kg/kg). Category: BULK INGREDIENT.
Metronidazole Hydrochloride
metronidazole hydrochloride
Manufactured by PFIZER. Dosage form: INJECTABLE. Route: INJECTION. Active ingredients: METRONIDAZOLE HYDROCHLORIDE (EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**). Application: NDA018353.
Metronidazole Micronized
metronidazole micronized
Dosage form: POWDER. Active ingredients: METRONIDAZOLE (1 g/g). Category: BULK INGREDIENT.
Metronidazole Oral
metronidazole oral
11 DESCRIPTION LIKMEZ (metronidazole) oral suspension is a nitroimidazole antimicrobial. The chemical name of metronidazole is 2-methyl-5-nitro-1H-imidazole-1-ethanol. The structural formula is shown as: Metronidazole is a white to pale yellow crystalline powder with a molecular formula of C 6H 9N 3O 3and a molecular weight of 171.2 g/mole. The pKa of metronidazole is 14.44 ± 0.10. The pH of a 1% aqueous solution of metronidazole is 5.5-7.5.
Brands: Likmez
Metronidazole Topical
metronidazole topical
DESCRIPTION Metronidazole gel USP (topical), 0.75%, contains metronidazole, at a concentration of 7.5 mg per gram (0.75%) in a gel consisting of carbopol 980, edetate disodium, methylparaben, propylene glycol, propylparaben, purified water, and sodium hydroxide. Metronidazole is classified therapeutically as an antiprotozoal and anti-bacterial agent. Chemically, metronidazole is named 2-methyl-5-nitro-1H-imidazole-1- ethanol and has the following structure: Structure
Brands: Metronidazole
Metronidazole Vaginal Gel, 1.3 %
metronidazole vaginal gel, 1.3 %
11 DESCRIPTION Metronidazole vaginal gel contains 1.3% metronidazole, USP in a single-dose prefilled disposable applicator. It is intended for intravaginal use. Metronidazole is a nitroimidazole antimicrobial. Chemically, metronidazole is a 2-methyl-5-nitroimidazole-1-ethanol. Its structural formula is: The molecular formula is C 6 H 9 N 3 O 3 with a molecular weight of 171.16. Metronidazole vaginal gel is an aqueous gel containing metronidazole at a concentration of 13 mg/g (1.3%).
Brands: Metronidazole Vaginal Gel
Metyrapone
metyrapone
11 DESCRIPTION Metopirone (metyrapone capsules) is an adrenal steroid synthesis inhibitor, available as 250‑mg capsules for oral administration. Its chemical name is 2‑methyl‑1, 2‑di‑3‑pyridyl‑1‑propanone, and its structural formula is Metyrapone is a white to light amber, fine, crystalline powder, having a characteristic odor. It is sparingly soluble in water, and soluble in methanol and in chloroform. It forms water‑soluble salts with acids. Its molecular weight is 226.27.
Brands: Metopirone
Metyrosine
metyrosine
DESCRIPTION Metyrosine is (–)-α-methyl- L -tyrosine or (α-MPT). It has the following structural formula: Metyrosine USP is a white to off-white, crystalline compound of molecular weight 195.22. It is very slightly soluble in water, acetone, and methanol, and insoluble in chloroform and benzene. It is soluble in acidic aqueous solutions. It is also soluble in alkaline aqueous solutions but is subject to oxidative degradation under these conditions.
Brands: Metyrosine
Mevastatin
mevastatin
Dosage form: POWDER. Active ingredients: MEVASTATIN (1 kg/kg). Category: BULK INGREDIENT.
Mexiletine Hydrochloride
mexiletine hydrochloride
DESCRIPTION Mexiletine hydrochloride, USP is an orally active antiarrhythmic agent. It is a white to off-white crystalline powder with slightly bitter taste, freely soluble in water and in alcohol. Mexiletine hydrochloride, USP has a pKa of 9.2. The chemical name of mexiletine hydrochloride, USP is 1-methyl-2-(2,6-xylyloxy)ethylamine hydrochloride and its structural formula is: C 11 H 17 NO • HCl M.W.
Brands: Mexiletine Hydrochloride
Medical Disclaimer
This drug database is for informational purposes only. Drug information is sourced from the FDA National Drug Code Directory and Structured Product Labeling. Always consult with a healthcare provider before starting, stopping, or changing any medication.