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Omeprazole

NDC 55111-159 · Dr. Reddy's Laboratories Limited

Generic nameOmeprazole
Dosage formCAPSULE, DELAYED RELEASE
RouteORAL
Active ingredient(s)OMEPRAZOLE
Strength40 mg/1
Pharmacologic classCytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
Marketing categoryANDA

Packages

55111-159-01 — 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-159-01)

55111-159-05 — 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-159-05)

55111-159-10 — 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-159-10)

55111-159-30 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-159-30)

55111-159-78 — 10 BLISTER PACK in 1 CARTON (55111-159-78) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (55111-159-79)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 55111-157 — Omeprazole, 55111-158 — Omeprazole, 55111-643 — Omeprazole, 55111-644 — Omeprazole, 55111-645 — Omeprazole, 55154-2332 — Omeprazole, 55301-915 — Omeprazole, 55681-306 — OMEPRAZOLE, 55910-215 — Omeprazole, 55910-712 — omeprazole, 55910-713 — omeprazole, 55910-915 — 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.