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Omeprazole

NDC 51407-641 · Golden State Medical Supply, 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

51407-641-00 — 1 CAPSULE, DELAYED RELEASE in 1 PAIL (51407-641-00)

51407-641-01 — 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (51407-641-01)

51407-641-10 — 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (51407-641-10)

51407-641-90 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (51407-641-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 50268-657 — Omeprazole, 51407-287 — Omeprazole, 51407-664 — OMEPRAZOLE, 51407-813 — Omeprazole, 51407-814 — OMEPRAZOLE, 51407-943 — Omeprazole, 51655-061 — Omeprazole, 51655-452 — Omeprazole, 51655-893 — Omeprazole, 51660-029 — Omeprazole, 53041-663 — Omeprazole, Sodium bicarbonate, 53041-664 — 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.