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Acid Reducer

NDC 80136-852 · NORTHEAST PHARMA

Generic nameOmeprazole
Dosage formTABLET, DELAYED RELEASE
RouteORAL
Active ingredient(s)OMEPRAZOLE MAGNESIUM
Strength20 mg/1
Pharmacologic classCytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
Marketing categoryANDA

Packages

80136-852-03 — 3 BOTTLE in 1 CARTON (80136-852-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

80136-852-42 — 3 BLISTER PACK in 1 CARTON (80136-852-42) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67091-464 — Omeprazole, 68016-760 — Omeprazole Magnesium, 69618-054 — Omeprazole, 69842-027 — Omeprazole Magnesium, 69842-941 — Omeprazole, 70000-0232 — Omeprazole Magnesium, 70000-0521 — Omeprazole, 70515-610 — omeprazole magnesium, 70515-625 — omeprazole magnesium, 72288-023 — Omeprazole magnesium, 72288-409 — Omeprazole, 79481-0061 — Omeprazole, 79481-0281 — Omeprazole magnesium, 79481-3023 — Omeprazole, 79903-112 — Omeprazole magnesium, 79903-377 — Omeprazole, 83324-117 — Omeprazole Magnesium, 84126-300 — OMEPRAZOLE MAGNESIUM, 84126-301 — OMEPRAZOLE MAGNESIUM, 85828-731 — Omeprazole 20 mg, +56 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.