PANTOPRAZOLE SODIUM

Product NDC

68071-3038

11-digit product format

680713038

Labeler code

68071

Product ID

68071-3038_49db4bc2-2cf6-3466-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

PANTOPRAZOLE

Dosage form

TABLET, DELAYED RELEASE

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA202882

Marketing category

ANDA

Marketing start

2014-09-10

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