NDC 71335-0551 – Pantoprazole Sodium

Pantoprazole Sodium 40 mg/1 · Tablet, Delayed Release · Oral

Human Prescription Drug

Product NDC71335-0551

Product details

Brand name
Pantoprazole Sodium
Generic name
Pantoprazole
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA202882
Marketed since
September 10, 2014
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
71335-0551-190 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-1)Sep 15, 2020
71335-0551-230 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-2)Jul 31, 2020
71335-0551-360 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-3)Jun 17, 2020
71335-0551-458 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-4)Apr 3, 2024
71335-0551-514 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-5)Mar 10, 2022
71335-0551-6100 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-6)Apr 3, 2024
71335-0551-710 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-7)Apr 3, 2024
71335-0551-8120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-8)Apr 3, 2024
71335-0551-9180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0551-9)Apr 3, 2024

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