Omeprazole

NDC 0781-2859 · Sandoz Inc

Generic nameOmeprazole

Dosage formCAPSULE, DELAYED RELEASE

RouteORAL

Active ingredient(s)OMEPRAZOLE

Strength10 mg/1

Pharmacologic classCytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]

Marketing categoryANDA

Packages

0781-2859-01 — 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2859-01)

0781-2859-10 — 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2859-10)

0781-2859-31 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2859-31)

0781-2859-92 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2859-92)

FDA lists these products with the same active ingredient.

0363-0915 — Omeprazole, 0363-1607 — Omeprazole, 0363-1819 — omeprazole, 0363-6101 — omeprazole, 0536-1448 — Omeprazole, 0615-8079 — Omeprazole, 0615-8406 — Omeprazole, 0781-2234 — Omeprazole, 0781-2785 — Omeprazole, 0781-2790 — Omeprazole, 0781-2868 — Omeprazole, 0904-6917 — Omeprazole, 11673-018 — Omeprazole, 11673-212 — omeprazole, 11673-346 — omeprazole, 11673-915 — Omeprazole, 11822-0453 — Omeprazole, 11822-1190 — omeprazole, 16714-123 — Omeprazole, 16714-630 — 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.