Omeprazole

NDC 70700-150 · Xiromed, LLC

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

70700-150-00 — 1 CAPSULE, DELAYED RELEASE in 1 PAIL (70700-150-00)

70700-150-01 — 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70700-150-01)

70700-150-10 — 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70700-150-10)

70700-150-30 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70700-150-30)

FDA lists these products with the same active ingredient.

70000-0723 — Omeprazole, 70518-0199 — Omeprazole, 70518-2251 — Omeprazole, 70518-3278 — Omeprazole, 70518-4177 — Omeprazole, 70677-0148 — Omeprazole, 70677-1098 — Omeprazole, 70677-1104 — Omeprazole, 70677-1275 — Omeprazole, 70700-149 — 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, 71335-0332 — 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.