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Omeprazole

NDC 68071-2243 · 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

68071-2243-7 — 7 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-2243-7)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65841-761 — Omeprazole, 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, 68071-2262 — 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, +295 more

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