Pantoprazole Sodium

Product NDC

63629-3353

11-digit product format

636293353

Labeler code

63629

Product ID

63629-3353_e0de4498-cabf-44b6-b067-52756eef0577

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Pantoprazole Sodium

Dosage form

TABLET, DELAYED RELEASE

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA077056

Marketing category

ANDA

Marketing start

2007-12-19

Marketing end

0000-00-00

Substance

PANTOPRAZOLE SODIUM

Active strength

40 mg/1

Pharmacologic classes

Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record