Omeprazole

NDC 68788-8864 · Preferred 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

68788-8864-1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8864-1)

68788-8864-2 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8864-2)

68788-8864-3 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8864-3)

68788-8864-4 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8864-4)

68788-8864-6 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8864-6)

68788-8864-8 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8864-8)

68788-8864-9 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8864-9)

FDA lists these products with the same active ingredient.

68462-396 — Omeprazole, 68462-397 — Omeprazole, 68682-102 — omeprazole, sodium bicarbonate, 68682-104 — omeprazole, sodium bicarbonate, 68682-990 — omeprazole, sodium bicarbonate, 68788-4104 — Omeprazole, 68788-6881 — Omeprazole, 68788-6995 — Omeprazole, 68788-8771 — Omeprazole, 68788-8805 — Omeprazole, 69097-913 — omeprazole sodium bicarbonate, 69097-914 — omeprazole sodium bicarbonate, 69168-476 — Omeprazole, 69230-318 — Omeprazole, 69367-196 — Omeprazole and Sodium Bicarbonate, 69842-661 — omeprazole, 69842-791 — omeprazole, 70000-0381 — omeprazole, 70000-0723 — Omeprazole, 70518-0199 — 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.