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Omeprazole

NDC 71335-1746 · Bryant Ranch Prepack

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

71335-1746-0 7 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1746-0)

71335-1746-1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1746-1)

71335-1746-2 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1746-2)

71335-1746-3 56 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1746-3)

71335-1746-4 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1746-4)

71335-1746-5 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1746-5)

71335-1746-6 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1746-6)

71335-1746-7 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1746-7)

71335-1746-8 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1746-8)

71335-1746-9 28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1746-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71205-613 — Omeprazole, 71205-907 — Omeprazole, 71205-985 — Omeprazole and Sodium Bicarbonate, 71335-0299 — Omeprazole, 71335-0332 — Omeprazole, 71335-0569 — Omeprazole, 71335-1395 — Omeprazole, 71335-1532 — omeprazole, 71335-1636 — Omeprazole, 71335-1639 — 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, 71610-876 — 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.