Pantoprazole Sodium

Product NDC

42291-659

11-digit product format

422910659

Labeler code

42291

Product ID

42291-659_9daec180-8af8-1269-e053-2a95a90a8bdb

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Pantoprazole Sodium

Dosage form

TABLET, DELAYED RELEASE

Route

ORAL

Labeler

AvKARE, Inc.

Application

ANDA077056

Marketing category

ANDA

Marketing start

2016-02-22

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

2021-12-31

Current FDA listing

Historical FDA.report record