Rabeprazole sodium

Product NDC

50436-1070

11-digit product format

504361070

Labeler code

50436

Product ID

50436-1070_489f031d-6996-404f-bdb6-07783fd61ea2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Rabeprazole sodium

Dosage form

TABLET, DELAYED RELEASE

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA202376

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

2019-12-31

Current FDA listing

Historical FDA.report record