Pantoprazole Sodium

Product NDC

63629-3353

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Pantoprazole Sodium

Dosage form

TABLET, DELAYED RELEASE

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA077056

Marketing category

ANDA

Substance

PANTOPRAZOLE SODIUM

Current FDA listing

Historical FDA.report record