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Omeprazole

NDC 55681-306 · Twin Med LLC

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

55681-306-14 — 1 BOTTLE in 1 CARTON (55681-306-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

55681-306-42 — 3 BOTTLE in 1 CARTON (55681-306-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 55910-215 — Omeprazole, 55910-712 — omeprazole, 55910-713 — omeprazole, 55910-915 — Omeprazole, 56062-401 — Omeprazole, 56062-915 — Omeprazole, 57237-160 — Omeprazole, 57237-161 — Omeprazole, 57237-162 — Omeprazole, 57483-840 — omeprazole, +295 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.