Omeprazole

NDC 55111-644 · Dr. Reddy's Laboratories Limited

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

55111-644-01 — 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-644-01)

55111-644-05 — 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-644-05)

55111-644-10 — 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-644-10)

55111-644-30 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-644-30)

55111-644-77 — 1 BLISTER PACK in 1 CARTON (55111-644-77) / 7 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK

FDA lists these products with the same active ingredient.

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, 55111-159 — Omeprazole, 55111-643 — 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, 56062-401 — Omeprazole, 56062-915 — 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.