Omeprazole

NDC 68071-2262 · NuCare Pharmaceuticals,Inc.

Generic nameOmeprazole

Dosage formCAPSULE, DELAYED RELEASE

RouteORAL

Active ingredient(s)OMEPRAZOLE

Strength20 mg/1

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

Marketing categoryANDA

Packages

68071-2262-3 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-2262-3)

FDA lists these products with the same active ingredient.

67046-1509 — Omeprazole, 67296-1939 — Omeprazole, 67296-2183 — Omeprazole, 68001-441 — Omeprazole, 68012-052 — omeprazole and sodium bicarbonate, 68012-054 — omeprazole and sodium bicarbonate, 68012-102 — omeprazole and sodium bicarbonate, 68012-104 — omeprazole and sodium bicarbonate, 68071-2199 — Omeprazole, 68071-2243 — omeprazole, 68071-2741 — Omeprazole, 68071-3007 — Omeprazole, 68071-3733 — Omeprazole, 68071-4024 — Omeprazole, 68071-4025 — omeprazole, 68071-4906 — omeprazole, 68084-128 — Omeprazole, 68196-700 — Omeprazole, 68196-915 — Omeprazole, 68382-411 — 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.