NDC 71335-0291 – Pantoprazole Sodium

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

Human Prescription Drug

Product NDC71335-0291

Product details

Brand name
Pantoprazole Sodium
Generic name
Pantoprazole
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA205119
Marketed since
June 20, 2016
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

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

Package NDC codes (9)

Package NDCDescriptionSince
71335-0291-160 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-1)Apr 29, 2022
71335-0291-230 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-2)May 24, 2022
71335-0291-390 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-3)Jun 28, 2022
71335-0291-456 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-4)Jun 28, 2022
71335-0291-528 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-5)Jun 28, 2022
71335-0291-610 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-6)Jun 28, 2022
71335-0291-7120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-7)Jun 28, 2022
71335-0291-8180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-8)Jun 28, 2022
71335-0291-93 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-9)Jun 28, 2022

Other Pantoprazole Sodium products