Rabeprazole Sodium

Product NDC

71335-0636

11-digit product format

713350636

Labeler code

71335

Product ID

71335-0636_2854ec94-9258-4703-b3bb-6bb1853de818

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

RABEPRAZOLE SODIUM

Dosage form

TABLET, DELAYED RELEASE

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA204237

Marketing category

ANDA

Marketing start

2017-06-01

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