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care one omeprazole

NDC 41520-915 · American Sales Company

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

41520-915-03 — 3 BOTTLE in 1 CARTON (41520-915-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

41520-915-55 — 3 CARTON in 1 CARTON (41520-915-55) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK

41520-915-74 — 14 BLISTER PACK in 1 CARTON (41520-915-74) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 41250-938 — Omeprazole, sodium bicarbonate, 41520-802 — Omeprazole, 41520-939 — omeprazole, 42507-164 — omeprazole, 42507-414 — Omeprazole, 42507-915 — Omeprazole, 42708-158 — Omeprazole, 42708-159 — Omeprazole, 42708-170 — Omeprazole, 42708-199 — Omeprazole, 43063-743 — Omeprazole, 43353-829 — 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.