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Omeprazole

NDC 51660-029 · OHM LABORATORIES 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 categoryANDA

Packages

51660-029-14 — 1 BOTTLE in 1 CARTON (51660-029-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

51660-029-27 — 2 BOTTLE in 1 CARTON (51660-029-27) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

51660-029-44 — 3 BOTTLE in 1 CARTON (51660-029-44) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50268-657 — Omeprazole, 51407-287 — Omeprazole, 51407-641 — Omeprazole, 51407-664 — OMEPRAZOLE, 51407-813 — Omeprazole, 51407-814 — OMEPRAZOLE, 51407-943 — Omeprazole, 51655-061 — Omeprazole, 51655-452 — Omeprazole, 51655-893 — Omeprazole, 53041-663 — Omeprazole, Sodium bicarbonate, 53041-664 — Omeprazole, Sodium bicarbonate, 55111-157 — Omeprazole, 55111-158 — Omeprazole, 55111-159 — Omeprazole, 55111-643 — Omeprazole, 55111-644 — Omeprazole, 55111-645 — Omeprazole, 55154-2332 — Omeprazole, 55301-915 — 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.