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Omeprazole

NDC 71205-613 · Proficient Rx LP

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

71205-613-06 — 6 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-613-06)

71205-613-14 — 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-613-14)

71205-613-30 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-613-30)

71205-613-60 — 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-613-60)

71205-613-90 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-613-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70677-1098 — Omeprazole, 70677-1104 — Omeprazole, 70677-1275 — Omeprazole, 70700-149 — Omeprazole, 70700-150 — Omeprazole, 70700-151 — Omeprazole, 70954-797 — Omeprazole and Sodium Bicarbonate, 70954-798 — Omeprazole and Sodium Bicarbonate, 71205-157 — omeprazole, 71205-501 — Omeprazole, 71205-907 — 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, 71335-1746 — 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.