NDC 71335-0332 – Omeprazole

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

Human Prescription Drug

Product NDC71335-0332

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Bryant Ranch Prepack
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA075576
Marketed since
January 21, 2009
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
71335-0332-07 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-0)May 28, 2024
71335-0332-130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-1)Jul 16, 2018
71335-0332-260 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-2)Mar 25, 2020
71335-0332-356 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-3)May 28, 2024
71335-0332-490 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-4)May 8, 2020
71335-0332-520 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-5)Jun 3, 2020
71335-0332-615 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-6)Jul 6, 2018
71335-0332-7120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-7)Mar 12, 2020
71335-0332-8100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-8)May 28, 2024
71335-0332-928 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-9)May 28, 2024

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