NDC 71335-1639 – Omeprazole

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

Human Prescription Drug

Product NDC71335-1639

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, 2027
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (10)

Package NDCDescriptionSince
71335-1639-07 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1639-0)Jun 30, 2022
71335-1639-130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1639-1)Jun 30, 2022
71335-1639-260 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1639-2)Jun 30, 2022
71335-1639-356 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1639-3)Jun 30, 2022
71335-1639-490 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1639-4)Jun 17, 2020
71335-1639-520 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1639-5)Jun 30, 2022
71335-1639-615 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1639-6)Jun 30, 2022
71335-1639-7120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1639-7)Jun 30, 2022
71335-1639-8100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1639-8)Jun 30, 2022
71335-1639-928 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1639-9)Jun 30, 2022

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