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Omeprazole

NDC 70518-2251 · REMEDYREPACK INC.

Generic nameOmeprazole
Dosage formCAPSULE, 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 categoryANDA

Packages

70518-2251-5 — 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-2251-5)

70518-2251-6 — 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-2251-6)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69097-913 — omeprazole sodium bicarbonate, 69097-914 — omeprazole sodium bicarbonate, 69168-476 — Omeprazole, 69230-318 — Omeprazole, 69367-196 — Omeprazole and Sodium Bicarbonate, 69842-661 — omeprazole, 69842-791 — omeprazole, 70000-0381 — omeprazole, 70000-0723 — Omeprazole, 70518-0199 — Omeprazole, 70518-3278 — Omeprazole, 70518-4177 — Omeprazole, 70677-0148 — Omeprazole, 70677-1098 — Omeprazole, 70677-1104 — Omeprazole, 70677-1275 — Omeprazole, 70700-149 — Omeprazole, 70700-150 — Omeprazole, 70700-151 — Omeprazole, 70954-797 — Omeprazole and Sodium Bicarbonate, +295 more

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