Chlordiazepoxide Hydrochloride

Product NDC

68071-2145

11-digit product format

680712145

Labeler code

68071

Product ID

68071-2145_46ef7319-deb6-6122-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Chlordiazepoxide Hydrochloride

Dosage form

CAPSULE, GELATIN COATED

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA085472

Marketing category

ANDA

Marketing start

2010-05-15

Marketing end

0000-00-00

Substance

CHLORDIAZEPOXIDE HYDROCHLORIDE

Active strength

10 mg/1

Pharmacologic classes

Benzodiazepine [EPC],Benzodiazepines [CS]

DEA schedule

CIV

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record