NDC 71335-1165 – Pantoprazole Sodium

Pantoprazole Sodium 20 mg/1 · Tablet, Delayed Release · Oral

Human Prescription Drug

Product NDC71335-1165

Product details

Brand name
Pantoprazole Sodium
Generic name
Pantoprazole Sodium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA202038
Marketed since
September 28, 2012
Listing expires
December 31, 2027
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Pantoprazole Sodium →

Package NDC codes (8)

Package NDCDescriptionSince
71335-1165-160 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1165-1)Apr 18, 2019
71335-1165-230 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1165-2)Mar 21, 2019
71335-1165-390 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1165-3)Mar 21, 2019
71335-1165-456 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1165-4)May 17, 2024
71335-1165-528 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1165-5)May 17, 2024
71335-1165-610 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1165-6)May 17, 2024
71335-1165-7120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1165-7)May 17, 2024
71335-1165-8180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1165-8)May 17, 2024

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