Chlordiazepoxide Hydrochloride

Product NDC

55289-061

11-digit product format

552890061

Labeler code

55289

Product ID

55289-061_531d01ec-b56d-44d6-e054-00144ff88e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Chlordiazepoxide Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

Application

ANDA083116

Marketing category

ANDA

Marketing start

1990-09-30

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record