Rabeprazole Sodium

Product NDC

0378-6709

11-digit product format

003786709

Labeler code

0378

Product ID

0378-6709_164627e8-c25a-4667-a1dd-1a2e33f3e035

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

rabeprazole

Dosage form

TABLET, DELAYED RELEASE

Route

ORAL

Labeler

Mylan Pharmaceuticals Inc.

Application

ANDA076885

Marketing category

ANDA

Marketing start

2013-11-08

Marketing end

2019-07-31

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

0000-00-00

Current FDA listing

Historical FDA.report record