Pantoprazole Sodium

Product NDC

55700-019

11-digit product format

557000019

Labeler code

55700

Product ID

55700-019_09d15cd0-5563-4291-8978-489186a6afdf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

pantoprazole sodium

Dosage form

TABLET, DELAYED RELEASE

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA090970

Marketing category

ANDA

Marketing start

2013-04-10

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

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record