Chlordiazepoxide Hydrochloride

Product NDC

42291-210

11-digit product format

422910210

Labeler code

42291

Product ID

42291-210_91c16c72-786d-a266-e053-2995a90a0cca

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Chlordiazepoxide Hydrochloride

Dosage form

CAPSULE, GELATIN COATED

Route

ORAL

Labeler

AvKARE, Inc.

Application

ANDA085461

Marketing category

ANDA

Marketing start

2011-03-14

Marketing end

0000-00-00

Substance

CHLORDIAZEPOXIDE HYDROCHLORIDE

Active strength

5 mg/1

Pharmacologic classes

Benzodiazepine [EPC],Benzodiazepines [CS]

DEA schedule

CIV

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record