Omeprazole

NDC 71335-0332 · 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

71335-0332-0 7 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-0)

71335-0332-1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-1)

71335-0332-2 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-2)

71335-0332-3 56 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-3)

71335-0332-4 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-4)

71335-0332-5 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-5)

71335-0332-6 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-6)

71335-0332-7 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-7)

71335-0332-8 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-8)

71335-0332-9 28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-9)

FDA lists these products with the same active ingredient.

70700-150 — Omeprazole, 70700-151 — Omeprazole, 70954-797 — Omeprazole and Sodium Bicarbonate, 70954-798 — Omeprazole and Sodium Bicarbonate, 71205-157 — omeprazole, 71205-501 — Omeprazole, 71205-613 — Omeprazole, 71205-907 — Omeprazole, 71205-985 — Omeprazole and Sodium Bicarbonate, 71335-0299 — Omeprazole, 71335-0569 — Omeprazole, 71335-1395 — Omeprazole, 71335-1532 — omeprazole, 71335-1636 — Omeprazole, 71335-1639 — Omeprazole, 71335-1746 — omeprazole, 71335-1851 — Omeprazole, 71335-1852 — Omeprazole, 71335-9609 — Omeprazole, 71335-9744 — Omeprazole, +295 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.