DIAZEPAM

Product NDC

61919-377

11-digit product format

619190377

Labeler code

61919

Product ID

61919-377_5dc82a54-d435-2b58-e053-2991aa0a7031

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

DIAZEPAM

Dosage form

TABLET

Route

ORAL

Labeler

DIRECT RX

Application

ANDA077749

Marketing category

ANDA

Marketing start

2017-11-01

Marketing end

0000-00-00

Substance

DIAZEPAM

Active strength

10 mg/1

Pharmacologic classes

Benzodiazepine [EPC],Benzodiazepines [CS]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record