NDC 71335-0299 – Omeprazole

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

Human Prescription Drug

Product NDC71335-0299

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Bryant Ranch Prepack
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA091672
Marketed since
October 31, 2014
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
71335-0299-160 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0299-1)Mar 21, 2018
71335-0299-230 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0299-2)Mar 22, 2018
71335-0299-320 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0299-3)Nov 5, 2018
71335-0299-490 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0299-4)May 1, 2018
71335-0299-514 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0299-5)May 11, 2018
71335-0299-6120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0299-6)May 2, 2022
71335-0299-7100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0299-7)Oct 14, 2020
71335-0299-8180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0299-8)May 2, 2022

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