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members mark omeprazole

NDC 68196-915 · Sam's West Inc

Generic nameOmeprazole
Dosage formTABLET, 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 categoryNDA

Packages

68196-915-55 — 3 CARTON in 1 CARTON (68196-915-55) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-2243 — 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, 68382-411 — Omeprazole, 68382-412 — Omeprazole, 68382-500 — Omeprazole, 68391-103 — omeprazole, 68391-915 — Omeprazole, 68462-395 — Omeprazole, 68462-396 — Omeprazole, 68462-397 — Omeprazole, 68682-102 — omeprazole, sodium bicarbonate, 68682-104 — omeprazole, sodium bicarbonate, +295 more

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