Rabeprazole sodium

Product NDC

68071-2173

11-digit product format

680712173

Labeler code

68071

Product ID

68071-2173_504b36fb-83bd-26e3-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Rabeprazole sodium

Dosage form

TABLET, DELAYED RELEASE

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

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

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record