NDC 71335-1429 – Pantoprazole Sodium

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

Human Prescription Drug

Product NDC71335-1429

Product details

Brand name
Pantoprazole Sodium
Generic name
Pantoprazole sodium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA090970
Marketed since
January 19, 2011
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
71335-1429-190 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1429-1)Dec 9, 2019
71335-1429-230 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1429-2)Dec 19, 2019
71335-1429-360 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1429-3)Jan 20, 2020
71335-1429-458 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1429-4)May 20, 2024
71335-1429-514 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1429-5)May 20, 2024
71335-1429-6100 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1429-6)May 20, 2024
71335-1429-710 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1429-7)May 20, 2024
71335-1429-8120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1429-8)May 20, 2024
71335-1429-9180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1429-9)May 20, 2024

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