Pantoprazole Sodium

Product NDC

63187-551

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Pantoprazole Sodium

Dosage form

TABLET, DELAYED RELEASE

Route

ORAL

Labeler

Proficient Rx LP

Application

ANDA077056

Marketing category

ANDA

Substance

PANTOPRAZOLE SODIUM

Current FDA listing

Historical FDA.report record