Omeprazole

NDC 72789-482 · PD-Rx Pharmaceuticals, 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

72789-482-14 — 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-482-14)

72789-482-30 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-482-30)

72789-482-60 — 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-482-60)

72789-482-90 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-482-90)

FDA lists these products with the same active ingredient.

72288-047 — omeprazole, 72288-123 — omeprazole, 72288-401 — Omeprazole, 72288-606 — Omeprazole, 72288-732 — Omeprazole, sodium bicarbonate, 72288-915 — Omeprazole, 72476-473 — omeprazole, 72559-014 — omeprazole, 72789-155 — omeprazole, 72789-257 — Omeprazole, 75907-138 — Omeprazole and Sodium Bicarbonate, 75907-237 — Omeprazole and Sodium Bicarbonate, 76162-470 — omeprazole, 76420-055 — Omeprazole, 76420-878 — Omeprazole, 76420-879 — Omeprazole, 79481-0075 — omeprazole, 79903-013 — Omeprazole, sodium bicarbonate, 79903-113 — omeprazole, 79903-305 — 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.