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Olmesartan Medoxomil and Hydrochlorothiazide

NDC 65862-779 · Aurobindo Pharma Limited

Generic nameOlmesartan Medoxomil and Hydrochlorothiazide
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)OLMESARTAN MEDOXOMIL, HYDROCHLOROTHIAZIDE
Strength12.5; 20 mg/1; mg/1
Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
Marketing categoryANDA

Packages

65862-779-30 — 30 TABLET, FILM COATED in 1 BOTTLE (65862-779-30)

65862-779-78 — 10 BLISTER PACK in 1 CARTON (65862-779-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-779-10)

65862-779-90 — 90 TABLET, FILM COATED in 1 BOTTLE (65862-779-90)

65862-779-99 — 1000 TABLET, FILM COATED in 1 BOTTLE (65862-779-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65862-548 — Valsartan and Hydrochlorothiazide, 65862-549 — Valsartan and Hydrochlorothiazide, 65862-550 — Valsartan and Hydrochlorothiazide, 65862-551 — Valsartan and Hydrochlorothiazide, 65862-629 — Irbesartan and Hydrochlorothiazide, 65862-630 — Irbesartan and Hydrochlorothiazide, 65862-631 — Irbesartan and Hydrochlorothiazide, 65862-741 — Olmesartan Medoxomil, 65862-742 — Olmesartan Medoxomil, 65862-743 — Olmesartan Medoxomil, 65862-780 — Olmesartan Medoxomil and Hydrochlorothiazide, 65862-781 — Olmesartan Medoxomil and Hydrochlorothiazide, 65862-834 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-835 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-836 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-837 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-838 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-854 — Amlodipine and Olmesartan Medoxomil, 65862-855 — Amlodipine and Olmesartan Medoxomil, 65862-856 — Amlodipine and Olmesartan Medoxomil, +1041 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.