NDC 71335-1532 – Omeprazole

Omeprazole 40 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC71335-1532

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Bryant Ranch Prepack
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA075410
Marketed since
January 23, 2009
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (8)

Package NDCDescriptionSince
71335-1532-160 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1532-1)Mar 13, 2020
71335-1532-230 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1532-2)Mar 17, 2020
71335-1532-320 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1532-3)Mar 10, 2022
71335-1532-490 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1532-4)Apr 24, 2020
71335-1532-514 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1532-5)Mar 16, 2020
71335-1532-6120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1532-6)Mar 10, 2022
71335-1532-7100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1532-7)Mar 1, 2021
71335-1532-8180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1532-8)Mar 10, 2022

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