Protonix

Product NDC

55154-4234

11-digit product format

551544234

Labeler code

55154

Product ID

55154-4234_b3ab36cf-7e71-4812-badf-529a6cde46e5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

pantoprazole sodium

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAVENOUS

Labeler

Cardinal Health

Application

NDA020988

Marketing category

NDA

Marketing start

2001-05-01

Marketing end

0000-00-00

Substance

PANTOPRAZOLE SODIUM

Active strength

40 mg/10mL

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record