NDC 71335-1851 – Omeprazole

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

Human Prescription Drug

Product NDC71335-1851

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Bryant Ranch Prepack
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA203270
Marketed since
August 19, 2015
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
71335-1851-160 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1851-1)May 19, 2021
71335-1851-230 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1851-2)May 19, 2021
71335-1851-320 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1851-3)Dec 11, 2024
71335-1851-490 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1851-4)May 20, 2021
71335-1851-514 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1851-5)Jun 7, 2021
71335-1851-6120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1851-6)Dec 11, 2024
71335-1851-7100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1851-7)Dec 11, 2024
71335-1851-8180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1851-8)Dec 11, 2024

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