Rabeprazole Sodium

Product NDC

68071-4353

11-digit product format

680714353

Labeler code

68071

Product ID

68071-4353_681c4972-b7a7-5c28-e053-2991aa0abf3c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

RABEPRAZOLE SODIUM

Dosage form

TABLET, DELAYED RELEASE

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

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