Clorazepate Dipotassium

Product NDC

63629-3859

11-digit product format

636293859

Labeler code

63629

Product ID

63629-3859_d42b3b3a-fe63-40d9-acc1-90a515a03969

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Clorazepate Dipotassium

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA075731

Marketing category

ANDA

Marketing start

2000-04-27

Marketing end

0000-00-00

Substance

CLORAZEPATE DIPOTASSIUM

Active strength

15 mg/1

Pharmacologic classes

Benzodiazepine [EPC],Benzodiazepines [CS]

DEA schedule

CIV

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record