Pantoprazole Sodium

Product NDC

63187-119

11-digit product format

631870119

Labeler code

63187

Product ID

63187-119_ef4687c8-6fe5-4c0e-9193-ce5af1f58f03

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Pantoprazole Sodium

Dosage form

TABLET, DELAYED RELEASE

Route

ORAL

Labeler

Proficient Rx LP

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

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record