NDC 76420-805 – Pantoprazole Sodium

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

Human Prescription Drug

Product NDC76420-805

Product details

Brand name
Pantoprazole Sodium
Generic name
Pantoprazole Sodium
Labeler
Asclemed USA, Inc.
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA202038
Marketed since
September 28, 2012
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
76420-805-1010 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-805-10)May 1, 2024
76420-805-3030 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-805-30)May 1, 2024
76420-805-6060 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-805-60)May 1, 2024
76420-805-9090 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-805-90)May 1, 2024

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