Diazepam

Product NDC

50436-3593

11-digit product format

504363593

Labeler code

50436

Product ID

50436-3593_dd6b33ce-17c8-45f6-90c7-35bbc2a6dfb3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

diazepam

Dosage form

TABLET

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA077749

Marketing category

ANDA

Marketing start

2006-03-31

Marketing end

2019-08-31

Substance

DIAZEPAM

Active strength

10 mg/1

Pharmacologic classes

Benzodiazepine [EPC],Benzodiazepines [CS]

DEA schedule

CIV

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record