Clorazepate Dipotassium

Product NDC

43063-350

11-digit product format

430630350

Labeler code

43063

Product ID

43063-350_5c51032b-f378-f68d-e053-2a91aa0a7540

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

clorazepate dipotassium

Dosage form

TABLET

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

Application

ANDA071858

Marketing category

ANDA

Marketing start

2010-07-29

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record