Rabeprazole Sodium

Product NDC

68788-8911

11-digit product format

687888911

Labeler code

68788

Product ID

68788-8911_4c3d4dbd-c440-49a8-a9d5-2596ab13f00a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Rabeprazole Sodium

Dosage form

TABLET, DELAYED RELEASE

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA076822

Marketing category

ANDA

Marketing start

2015-08-27

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