Clorazepate dipotassium

Product NDC

63629-3858

11-digit product format

636293858

Labeler code

63629

Product ID

63629-3858_1012b2db-17ff-4f67-abe9-bc48c5c2dc06

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Clorazepate dipotassium

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA076911

Marketing category

ANDA

Marketing start

2005-01-14

Marketing end

0000-00-00

Substance

CLORAZEPATE DIPOTASSIUM

Active strength

8 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