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Omeprazole

NDC 71610-876 · Aphena Pharma Solutions - Tennessee, LLC

Generic nameOmeprazole
Dosage formCAPSULE, DELAYED RELEASE
RouteORAL
Active ingredient(s)OMEPRAZOLE
Strength40 mg/1
Pharmacologic classCytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
Marketing categoryANDA

Packages

71610-876-53 — 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-876-53)

71610-876-60 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-876-60)

71610-876-70 — 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-876-70)

71610-876-80 — 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-876-80)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-1746 — omeprazole, 71335-1851 — Omeprazole, 71335-1852 — Omeprazole, 71335-9609 — Omeprazole, 71335-9744 — Omeprazole, 71610-248 — Omeprazole, 71610-280 — Omeprazole, 71610-663 — Omeprazole, 71610-688 — OMEPRAZOLE, 71610-875 — Omeprazole, 71610-880 — Omeprazole, 71610-912 — Omeprazole, 71610-942 — Omeprazole, 71610-963 — Omeprazole, 72036-981 — OMEPRAZOLE, 72162-1906 — omeprazole, sodium bicarbonate, 72162-2388 — Omeprazole, 72189-568 — Omeprazole/Sodiium Bicarbonate, 72288-047 — omeprazole, 72288-123 — 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.