NDC 60687-736 – Pantoprazole Sodium

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

Human Prescription Drug

Product NDC60687-736

Product details

Brand name
Pantoprazole Sodium
Generic name
Pantoprazole Sodium
Labeler
American Health Packaging
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA202038
Marketed since
July 5, 2023
Listing expires
December 31, 2027
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
60687-736-01100 BLISTER PACK in 1 CARTON (60687-736-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-736-11)Jul 5, 2023
60687-736-0980 BLISTER PACK in 1 CARTON (60687-736-09) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-736-11)Jul 5, 2023
60687-736-6550 BLISTER PACK in 1 CARTON (60687-736-65) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-736-11)Jul 5, 2023

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