NDC 71335-1852 – Omeprazole

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

Human Prescription Drug

Product NDC71335-1852

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 (10)

Package NDCDescriptionSince
71335-1852-07 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1852-0)Dec 11, 2024
71335-1852-130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1852-1)May 14, 2021
71335-1852-260 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1852-2)May 18, 2021
71335-1852-356 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1852-3)Dec 11, 2024
71335-1852-490 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1852-4)May 28, 2021
71335-1852-520 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1852-5)Oct 14, 2021
71335-1852-615 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1852-6)May 21, 2021
71335-1852-7120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1852-7)Jun 21, 2021
71335-1852-8100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1852-8)Dec 22, 2021
71335-1852-928 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1852-9)Dec 11, 2024

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