NDC 71335-9744 – Omeprazole

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

Human Prescription Drug

Product NDC71335-9744

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Bryant Ranch Prepack
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA091352
Marketed since
November 23, 2012
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
71335-9744-160 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9744-1)Jul 10, 2023
71335-9744-230 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9744-2)Jul 10, 2023
71335-9744-320 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9744-3)Jul 10, 2023
71335-9744-490 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9744-4)Jul 10, 2023
71335-9744-514 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9744-5)Jul 10, 2023
71335-9744-6120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9744-6)Jul 10, 2023
71335-9744-7100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9744-7)Jul 10, 2023
71335-9744-8180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9744-8)Jul 10, 2023

Other Omeprazole products