Rabeprazole Sodium

Product NDC

63187-158

11-digit product format

631870158

Labeler code

63187

Product ID

63187-158_0ff74492-aee6-4713-b182-1e4fdd7beae4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

rabeprazole

Dosage form

TABLET, DELAYED RELEASE

Route

ORAL

Labeler

Proficient Rx LP

Application

ANDA076885

Marketing category

ANDA

Marketing start

2013-11-08

Marketing end

0000-00-00

Substance

RABEPRAZOLE 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