NDC 71335-1395 – Omeprazole

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

Human Prescription Drug

Product NDC71335-1395

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
January 21, 2009
Marketing end
January 31, 2027
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (8)

Package NDCDescriptionSince
71335-1395-160 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1395-1)Feb 1, 2012
71335-1395-230 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1395-2)Feb 1, 2012
71335-1395-320 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1395-3)Feb 1, 2012
71335-1395-490 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1395-4)Feb 1, 2012
71335-1395-514 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1395-5)Feb 1, 2012
71335-1395-6120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1395-6)Feb 1, 2012
71335-1395-7100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1395-7)Feb 1, 2012
71335-1395-8180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1395-8)Feb 1, 2012

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