Pantoprazole Sodium

Product NDC

70518-1264

11-digit product format

705181264

Labeler code

70518

Product ID

70518-1264_91160a86-cde9-48e5-e053-2a95a90ad849

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

pantoprazole sodium

Dosage form

TABLET, DELAYED RELEASE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA090970

Marketing category

ANDA

Marketing start

2018-06-19

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