Drug & Medication Database
Browse 18,617 FDA-approved medications with detailed information about uses, dosage, side effects, and interactions.
Olmesartan Medoxomil
olmesartan medoxomil
11 DESCRIPTION Olmesartan medoxomil,USP a prodrug, is hydrolyzed to olmesartan during absorption from the gastrointestinal tract. Olmesartan is a selective AT1 subtype angiotensin II receptor antagonist. Olmesartan medoxomil is described chemically as 2,3-dihydroxy-2-butenyl 4-(1 hydroxy-1-methylethyl)-2-propyl-1-[p-(o-1H-tetrazol-5-ylphenyl)benzyl]imidazole5-carboxylate, cyclic 2,3-carbonate.
Brands: Olmesartan Medoxomil
Olmesartan Medoxomil (process-ii)
olmesartan medoxomil (process-ii)
Dosage form: POWDER. Active ingredients: OLMESARTAN MEDOXOMIL (50 kg/50kg). Category: BULK INGREDIENT.
Olmesartan Medoxomil / Amlodipine Besylate / Hydrochlorothiazide
olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
Fixed combination tablet containing olmesartan medoxomil, amlodipine besylate, and hydrochlorothiazide for the treatment of hypertension.
Brands: Olmesartan Medoxomil / Amlodipine Besylate / Hydrochlorothiazide
Olmesartan Medoxomil And Amlodipine Besylate And Hydrochlorothiazide
olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide
11 DESCRIPTION Olmesartan medoxomil, amlodipine, and hydrochlorothiazide tablets provided as a tablet for oral administration, is a fixed combination of olmesartan medoxomil (ARB), amlodipine (CCB), and hydrochlorothiazide (thiazide diuretic). Olmesartan medoxomil, a prodrug, is hydrolyzed to olmesartan during absorption from the gastrointestinal tract.
Brands: Olmesartan Medoxomil And Amlodipine Besylate And Hydrochlorothiazide
Olmesartan Medoxomil And Hydrochlorothiazide
olmesartan medoxomil and hydrochlorothiazide
Combination tablet containing olmesartan medoxomil and hydrochlorothiazide for the treatment of hypertension.
Brands: Olmesartan Medoxomil And Hydrochlorothiazide
Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide
olmesartan medoxomil, amlodipine and hydrochlorothiazide
11 DESCRIPTION Olmesartan medoxomil, amlodipine and hydrochlorothiazide provided as a tablet for oral administration, is a fixed combination of olmesartan medoxomil (ARB), amlodipine (CCB), and hydrochlorothiazide (thiazide diuretic). Olmesartan medoxomil, a prodrug, is hydrolyzed to olmesartan during absorption from the gastrointestinal tract.
Brands: Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide
Olmesartan Medoxomil, Amlodipine Besylate And Hydrochlorothiazide
olmesartan medoxomil, amlodipine besylate and hydrochlorothiazide
11 DESCRIPTION Olmesartan medoxomil, amlodipine and hydrochlorothiazide provided as a tablet for oral administration, is a fixed combination of olmesartan medoxomil (ARB), amlodipine (CCB), and hydrochlorothiazide (thiazide diuretic). Olmesartan medoxomil USP, a prodrug, is hydrolyzed to olmesartan during absorption from the gastrointestinal tract.
Brands: Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide
Olmesartan Medoxomil-hydrochlorothiazide
olmesartan medoxomil-hydrochlorothiazide
11 DESCRIPTION Olmesartan medoxomil and hydrochlorothiazide is a combination of an angiotensin II receptor antagonist (AT 1 subtype), olmesartan medoxomil, and a thiazide diuretic, hydrochlorothiazide (HCTZ). Olmesartan medoxomil is 2,3-dihydroxy-2-butenyl 4-(1-hydroxy-1-methylethyl)-2-propyl-1-[ p -( o -1 H -tetrazol-5-ylphenyl)benzyl]imidazole-5-carboxylate, cyclic 2,3-carbonate.
Brands: Olmesartan Medoxomil-hydrochlorothiazide
Olodaterol
olodaterol
Dosage form: POWDER. Active ingredients: OLODATEROL (15 kg/15kg). Category: BULK INGREDIENT.
Olodaterol Hcl
olodaterol hcl
Dosage form: POWDER. Active ingredients: OLODATEROL HYDROCHLORIDE (1 kg/kg). Category: BULK INGREDIENT.
Olodaterol Hydrochloride
olodaterol hydrochloride
Dosage form: POWDER. Active ingredients: OLODATEROL HYDROCHLORIDE (1 kg/kg). Category: BULK INGREDIENT.
Olodaterol Respimat Inhalation Spray
olodaterol respimat inhalation spray
11 DESCRIPTION The active moiety olodaterol is a selective beta 2 -adrenergic bronchodilator. The drug substance, olodaterol hydrochloride, is chemically described as 2H-1,4-Benzoxazin-3H(4H)-one, 6-hydroxy-8-[(1R)-1-hydroxy-2-[[2-(4-methoxyphenyl)-1,1-dimethylethyl]-amino]ethyl]-, monohydrochloride. Olodaterol hydrochloride is a white to off-white powder that is sparingly-slightly soluble in water and slightly soluble in ethanol.
Brands: Striverdi Respimat
Olopatadine
olopatadine
Drug Facts Active Ingredients Purpose Olopatadine (0.1%) (equivalent to olopatadine hydrochloride 0.111%) Antihistamine and Redness Reliever
Brands: Olopatadine
Olopatadine Hci
olopatadine hci
Dosage form: POWDER. Active ingredients: OLOPATADINE HYDROCHLORIDE (1 g/g). Category: BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING.
Olopatadine Hcl
olopatadine hcl
Purpose Antihistamine and redness reliever
Brands: Olopatadine Hcl
Olopatadine Hydrochloride
olopatadine hydrochloride
PURPOSE Antihistamine
Brands: Eye Allergy Itch Relief
Olopatadine Hydrochloride And Mometasone Furoate
olopatadine hydrochloride and mometasone furoate
11 DESCRIPTION RYALTRIS is a metered-dose manual nasal spray unit containing an aqueous suspension of a fixed‑dose combination of a histamine-1 (H1) receptor inhibitor (olopatadine hydrochloride) and a corticosteroid (mometasone furoate monohydrate). Olopatadine hydrochloride is a white, sparingly water‑soluble crystalline powder. The chemical name for olopatadine hydrochloride is 2‑[(11Z)-11-[3-(dimethylamino)propylidene]-6H-benzo[c][1]benzoxepin-2-yl]acetic acid hydrochloride.
Brands: Ryaltris
Olopatadine Hydrochloride Ophthalmic
olopatadine hydrochloride ophthalmic
Active Ingredient Purpose Olopatadine (0.1%). (equivalent to olopatadine hydrochloride 0.111%) Antihistamine and redness reliever
Brands: Olopatadine Hydrochloride
Olopatadine Hydrochloride Ophthalmic Solution
olopatadine hydrochloride ophthalmic solution
Purpose Antihistamine and Redness Reliever
Brands: Rugby Olopatadine Hydrochloride Ophthalmic Solution
Olsalazine Sodium
olsalazine sodium
11 DESCRIPTION The active ingredient in DIPENTUM (olsalazine sodium) is the sodium salt of a salicylate, disodium 3,3'-azobis (6-hydroxybenzoate) a compound that is effectively bioconverted to mesalamine (5-aminosalicylic acid,5-ASA), an aminosalicylate. Its empirical formula is C14H8N2Na2O6 with a molecular weight of 346.21. The structural formula is: Olsalazine sodium is a yellow crystalline powder, which melts with decomposition at 240°C.
Brands: Dipentum
Olutasidenib
olutasidenib
11 DESCRIPTION Olutasidenib is an isocitrate dehydrogenase-1 (IDH1) inhibitor. The chemical name is (S)-5-((1-(6-chloro-2-oxo-1,2-dihydroquinolin-3-yl)ethyl)amino)-1-methyl-6-oxo-1,6-dihydropyridine-2-carbonitrile. The chemical structure is: The molecular formula is C 18 H 15 ClN 4 O 2 and the molecular weight is 354.79 g/mol. Olutasidenib is a white to off-white to brown powder that is practically insoluble in aqueous solutions between pH 1.2 and 7.4.
Brands: Rezlidhia
Omacetaxine Mepesuccinate
omacetaxine mepesuccinate
Manufactured by TEVA PHARMS INTL. Dosage form: POWDER. Route: SUBCUTANEOUS. Active ingredients: OMACETAXINE MEPESUCCINATE (3.5MG/VIAL). Application: NDA203585.
Omadacycline
omadacycline
11 DESCRIPTION NUZYRA contains omadacycline tosylate, an aminomethylcycline which is a semisynthetic derivative of the tetracycline class of antibacterial drugs, for intravenous or oral administration. The chemical name of omadacycline tosylate is (4S,4aS,5aR,12aS)-4,7-bis(dimethylamino)-9-(2,2-dimethylpropylaminomethyl)-3,10,12,12a-tetrahydroxy-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydrotetracene-2-carboxamide, 4-methylbenzenesulfonate.
Brands: Nuzyra
Omadacycline Tosylate
omadacycline tosylate
Dosage form: POWDER. Active ingredients: OMADACYCLINE TOSYLATE (1 kg/kg). Category: BULK INGREDIENT.
Omalizumab
omalizumab
11 DESCRIPTION Omalizumab is a recombinant DNA-derived humanized IgG1κ monoclonal antibody that selectively binds to human immunoglobulin E (IgE). The antibody has a molecular weight of approximately 149 kiloDaltons. XOLAIR is produced by a Chinese hamster ovary cell suspension culture. XOLAIR (omalizumab) is administered as a subcutaneous (SC) injection and is available in prefilled syringe, autoinjector and in vials.
Brands: Xolair, Xolair Pfs, Xolair
Omalizumab-igec
omalizumab-igec
11 DESCRIPTION Omalizumab-igec is a recombinant DNA-derived humanized IgG1κ monoclonal antibody that selectively binds to human immunoglobulin E (IgE). The antibody has a molecular weight of approximately 149 kiloDaltons. Omalizumab-igec is produced by a Chinese hamster ovary cell suspension culture. Omalizumab-igec is administered as a subcutaneous (SC) injection and is available in prefilled syringes.
Brands: Omalizumab-igec
Omaveloxolone
omaveloxolone
11 DESCRIPTION SKYCLARYS contains omaveloxolone in immediate release capsules for oral administration available in a 50 mg strength. The chemical name of omaveloxolone is N-(2-cyano-3,12-dioxo-28-noroleana-1,9(11)-dien-17-yl)-2,2-difluoro-propanamide. Omaveloxolone is a white to off-white amorphous solid. The molecular formula is C 33 H 44 F 2 N 2 O 3 . Molecular weight is 554.72 g/mol.
Brands: Skyclarys
Omberacetam
omberacetam
Dosage form: POWDER. Active ingredients: OMBERACETAM (1 g/g). Category: BULK INGREDIENT.
Ombitasvir
ombitasvir
Manufactured by ABBVIE. Dosage form: TABLET, EXTENDED RELEASE. Route: ORAL. Active ingredients: DASABUVIR SODIUM (EQ 200MG BASE); OMBITASVIR (8.33MG); PARITAPREVIR (50MG); RITONAVIR (33.33MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**). Application: NDA208624.
Ombitasvir, Paritaprevir, Ritonavir
ombitasvir, paritaprevir, ritonavir
Manufactured by ABBVIE. Dosage form: TABLET. Route: ORAL. Active ingredients: DASABUVIR SODIUM (EQ 250MG BASE); OMBITASVIR, PARITAPREVIR, RITONAVIR (12.5MG, 75MG, 50MG). Application: NDA206619.
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.