Omeprazole

NDC 71335-1639 · 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

71335-1639-0 7 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1639-0)

71335-1639-1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1639-1)

71335-1639-2 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1639-2)

71335-1639-3 56 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1639-3)

71335-1639-4 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1639-4)

71335-1639-5 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1639-5)

71335-1639-6 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1639-6)

71335-1639-7 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1639-7)

71335-1639-8 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1639-8)

71335-1639-9 28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1639-9)

FDA lists these products with the same active ingredient.

71205-501 — Omeprazole, 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, 71335-1746 — 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, +295 more

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