equaline omeprazole

NDC 41163-915 · United Natural Foods, Inc. dba UNFI

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

41163-915-01 — 1 BOTTLE in 1 CARTON (41163-915-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

41163-915-30 — 2 CARTON in 1 CARTON (41163-915-30) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK

41163-915-55 — 3 CARTON in 1 CARTON (41163-915-55) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK

41163-915-74 — 14 BLISTER PACK in 1 CARTON (41163-915-74) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK

FDA lists these products with the same active ingredient.

31722-528 — omeprazole, 36800-121 — Omeprazole, 36800-601 — omeprazole, 36800-915 — Omeprazole, 37808-354 — omeprazole, 37808-401 — Omeprazole, 37808-732 — Omeprazole, sodium bicarbonate, 37808-915 — Omeprazole, 37835-001 — Omeprazole, 41163-634 — omeprazole, 41250-349 — omeprazole, 41250-401 — Omeprazole, 41250-915 — Omeprazole, 41250-938 — Omeprazole, sodium bicarbonate, 41520-802 — Omeprazole, 41520-915 — Omeprazole, 41520-939 — omeprazole, 42507-164 — omeprazole, 42507-414 — Omeprazole, 42507-915 — 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.