Diazepam

Product NDC

68788-6942

11-digit product format

687886942

Labeler code

68788

Product ID

68788-6942_ea788ea5-7082-4d1c-ab94-0224b6cabd88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Diazepam

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA071136

Marketing category

ANDA

Marketing start

2017-04-05

Marketing end

0000-00-00

Substance

DIAZEPAM

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