Chlordiazepoxide Hydrochloride

Product NDC

70518-0663

11-digit product format

705180663

Labeler code

70518

Product ID

70518-0663_8a12e5ca-a62f-6c3e-e053-2995a90a5738

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Chlordiazepoxide Hydrochloride

Dosage form

CAPSULE, GELATIN COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA085475

Marketing category

ANDA

Marketing start

2017-08-03

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

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record