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omeprazole

NDC 41250-915 · Meijer Distribution 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

41250-915-01 — 1 BOTTLE in 1 CARTON (41250-915-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

41250-915-02 — 2 BOTTLE in 1 CARTON (41250-915-02) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

41250-915-03 — 3 BOTTLE in 1 CARTON (41250-915-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

41250-915-55 — 3 CARTON in 1 CARTON (41250-915-55) / 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.

36800-915 — Omeprazole, 37808-354 — omeprazole, 37808-401 — Omeprazole, 37808-732 — Omeprazole, sodium bicarbonate, 37808-915 — Omeprazole, 37835-001 — Omeprazole, 41163-634 — omeprazole, 41163-915 — Omeprazole, 41250-349 — omeprazole, 41250-401 — Omeprazole, 41250-938 — Omeprazole, sodium bicarbonate, 41520-802 — Omeprazole, 41520-915 — Omeprazole, 41520-939 — omeprazole, 42507-164 — omeprazole, 42507-414 — Omeprazole, 42507-915 — Omeprazole, 42708-158 — Omeprazole, 42708-159 — Omeprazole, 42708-170 — 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.