up and up omeprazole

NDC 11673-018 · Target Corporation

Generic nameOmeprazole

Dosage formTABLET, 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 categoryNDA

Packages

11673-018-01 — 1 BOTTLE in 1 CARTON (11673-018-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

11673-018-03 — 3 BOTTLE in 1 CARTON (11673-018-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

FDA lists these products with the same active ingredient.

0363-6101 — omeprazole, 0536-1448 — Omeprazole, 0615-8079 — Omeprazole, 0615-8406 — Omeprazole, 0781-2234 — Omeprazole, 0781-2785 — Omeprazole, 0781-2790 — Omeprazole, 0781-2859 — Omeprazole, 0781-2868 — Omeprazole, 0904-6917 — Omeprazole, 11673-212 — omeprazole, 11673-346 — omeprazole, 11673-915 — Omeprazole, 11822-0453 — Omeprazole, 11822-1190 — omeprazole, 16714-123 — Omeprazole, 16714-630 — Omeprazole, 16714-634 — Omeprazole, 16714-714 — Omeprazole, 21130-128 — 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.