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Omeprazole

NDC 50090-7021 · A-S Medication Solutions

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

50090-7021-0 — 100 BLISTER PACK in 1 CARTON (50090-7021-0) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-3876 — Omeprazole, 50090-5111 — Omeprazole, 50090-5501 — Omeprazole, 50090-5901 — Omeprazole, 50090-5902 — Omeprazole, 50090-6720 — Omeprazole, 50090-6721 — Omeprazole, 50090-6888 — Omeprazole, 50090-7018 — Omeprazole, 50090-7019 — Omeprazole, 50090-7213 — Omeprazole, 50090-7214 — Omeprazole, 50090-7215 — Omeprazole, 50090-7366 — Omeprazole, 50090-7367 — Omeprazole, 50090-7472 — Omeprazole, 50090-7473 — Omeprazole, 50090-7474 — Omeprazole, 50228-363 — Omeprazole and Sodium Bicarbonate, 50228-364 — Omeprazole and 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.