NDC 71335-9609 – Omeprazole

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

Human Prescription Drug

Product NDC71335-9609

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Bryant Ranch Prepack
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA075757
Marketed since
July 1, 2019
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
71335-9609-07 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-0)Apr 3, 2024
71335-9609-130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-1)Jan 25, 2023
71335-9609-260 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-2)Dec 29, 2022
71335-9609-356 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-3)Apr 3, 2024
71335-9609-490 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-4)Feb 14, 2023
71335-9609-520 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-5)Apr 3, 2024
71335-9609-615 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-6)Apr 28, 2023
71335-9609-7120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-7)Dec 15, 2022
71335-9609-8100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-8)Apr 3, 2024
71335-9609-928 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9609-9)Apr 3, 2024

Other Omeprazole products