Pantoprazole Sodium

Product NDC

68788-9510

11-digit product format

687889510

Labeler code

68788

Product ID

68788-9510_1b4b8d3f-1386-408e-bfa2-c953fac95b9b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Pantoprazole Sodium

Dosage form

TABLET, DELAYED RELEASE

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA202038

Marketing category

ANDA

Marketing start

2014-02-18

Marketing end

0000-00-00

Substance

PANTOPRAZOLE SODIUM

Active strength

20 mg/1

Pharmacologic classes

Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record