NDC 71335-1636 – Omeprazole

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

Human Prescription Drug

Product NDC71335-1636

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Bryant Ranch Prepack
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA076048
Marketed since
November 11, 2003
Marketing end
January 31, 2027
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (10)

Package NDCDescriptionSince
71335-1636-07 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1636-0)Oct 31, 2024
71335-1636-130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1636-1)Oct 31, 2024
71335-1636-260 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1636-2)Oct 31, 2024
71335-1636-356 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1636-3)Oct 31, 2024
71335-1636-490 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1636-4)Oct 31, 2024
71335-1636-520 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1636-5)Oct 31, 2024
71335-1636-615 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1636-6)Oct 31, 2024
71335-1636-7120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1636-7)Oct 31, 2024
71335-1636-8100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1636-8)Oct 31, 2024
71335-1636-928 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1636-9)Oct 31, 2024

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