NDC 71335-0569 – Omeprazole

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

Human Prescription Drug

Product NDC71335-0569

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
71335-0569-07 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0569-0)Jun 26, 2006
71335-0569-130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0569-1)Jun 26, 2006
71335-0569-260 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0569-2)Jun 26, 2006
71335-0569-356 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0569-3)Jun 26, 2006
71335-0569-490 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0569-4)Jun 26, 2006
71335-0569-520 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0569-5)Jun 26, 2006
71335-0569-615 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0569-6)Jun 26, 2006
71335-0569-7120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0569-7)Jun 26, 2006
71335-0569-8100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0569-8)Jun 26, 2006
71335-0569-928 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0569-9)Jun 26, 2006

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