Chlordiazepoxide Hydrochloride

Product NDC

66267-051

11-digit product format

662670051

Labeler code

66267

Product ID

66267-051_3d95bbc1-cd7f-0eb4-e054-00144ff88e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Chlordiazepoxide Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA084769

Marketing category

ANDA

Marketing start

1976-07-02

Marketing end

0000-00-00

Substance

CHLORDIAZEPOXIDE HYDROCHLORIDE

Active strength

25 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