TopCare Omeprazole

NDC 36800-915 · Topco Associates LLC

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

36800-915-01 — 1 BOTTLE in 1 CARTON (36800-915-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

36800-915-03 — 3 BOTTLE in 1 CARTON (36800-915-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

36800-915-30 — 2 CARTON in 1 CARTON (36800-915-30) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK

36800-915-55 — 3 CARTON in 1 CARTON (36800-915-55) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK

36800-915-74 — 14 BLISTER PACK in 1 CARTON (36800-915-74) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK

FDA lists these products with the same active ingredient.

27241-032 — Omeprazole and Sodium Bicarbonate, 30142-394 — omeprazole, 30142-474 — omeprazole, 30142-557 — Omeprazole, 30142-593 — Omeprazole, 30142-992 — omeprazole, 31722-527 — omeprazole, 31722-528 — omeprazole, 36800-121 — Omeprazole, 36800-601 — omeprazole, 37808-354 — omeprazole, 37808-401 — Omeprazole, 37808-732 — Omeprazole, sodium bicarbonate, 37808-915 — Omeprazole, 37835-001 — Omeprazole, 41163-634 — omeprazole, 41163-915 — Omeprazole, 41250-349 — omeprazole, 41250-401 — Omeprazole, 41250-915 — 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.