NDC 71335-1746 – Omeprazole

Omeprazole 20 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC71335-1746

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
November 4, 2002
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (10)

Package NDCDescriptionSince
71335-1746-07 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1746-0)Feb 14, 2022
71335-1746-130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1746-1)Jan 11, 2021
71335-1746-260 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1746-2)Jan 11, 2021
71335-1746-356 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1746-3)Apr 19, 2021
71335-1746-490 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1746-4)Apr 2, 2021
71335-1746-520 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1746-5)May 3, 2021
71335-1746-615 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1746-6)Jun 8, 2021
71335-1746-7120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1746-7)Oct 7, 2021
71335-1746-8100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1746-8)Feb 14, 2022
71335-1746-928 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1746-9)Feb 14, 2022

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