Pantoprazole Sodium

Product NDC

42708-069

11-digit product format

427080069

Labeler code

42708

Product ID

42708-069_3a24b19b-c37c-42c4-9bac-79d85e7edde7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Pantoprazole Sodium

Dosage form

TABLET, DELAYED RELEASE

Route

ORAL

Labeler

QPharma Inc

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