Omeprazole

NDC 59651-003 · Aurobindo Pharma Limited

Generic nameOmeprazole

Dosage formCAPSULE, DELAYED RELEASE

RouteORAL

Active ingredient(s)OMEPRAZOLE

Strength40 mg/1

Pharmacologic classCytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]

Marketing categoryANDA

Packages

59651-003-01 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-003-01)

59651-003-03 3 BLISTER PACK in 1 CARTON (59651-003-03) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (59651-003-10)

59651-003-05 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-003-05)

59651-003-30 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-003-30)

59651-003-78 10 BLISTER PACK in 1 CARTON (59651-003-78) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (59651-003-10)

59651-003-90 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-003-90)

59651-003-99 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-003-99)

FDA lists these products with the same active ingredient.

57237-160 — Omeprazole, 57237-161 — Omeprazole, 57237-162 — Omeprazole, 57483-840 — omeprazole, 57896-659 — Omeprazole, 58602-725 — OMEPRAZOLE AND SODIUM BICARBONATE, 59640-047 — omeprazole, 59640-699 — Omeprazole, 59651-001 — Omeprazole, 59651-002 — Omeprazole, 59779-503 — Omeprazole, 59779-580 — Omeprazole, 59779-732 — Omeprazole, sodium bicarbonate, 60505-0065 — Omeprazole, 60505-0145 — Omeprazole, 60505-0146 — Omeprazole, 60505-3952 — Omeprazole, 60687-597 — Omeprazole, 60687-608 — Omeprazole, 60760-747 — Omeprazole, +295 more

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