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Good Sense Omeprazole

NDC 0113-0915 · L. Perrigo 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

0113-0915-01 — 1 BOTTLE in 1 CARTON (0113-0915-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

0113-0915-03 — 3 BOTTLE in 1 CARTON (0113-0915-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

0113-0915-30 — 2 CARTON in 1 CARTON (0113-0915-30) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK

0113-0915-55 — 3 CARTON in 1 CARTON (0113-0915-55) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK

0113-0915-74 — 14 BLISTER PACK in 1 CARTON (0113-0915-74) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0113-0058 — Omeprazole, sodium bicarbonate, 0113-0520 — omeprazole, 0113-1723 — Omeprazole, 0113-1803 — omeprazole, 0363-0007 — Omeprazole, 0363-0732 — Omeprazole, sodium bicarbonate, 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, 0781-2859 — Omeprazole, 0781-2868 — Omeprazole, 0904-6917 — Omeprazole, 11673-018 — 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.