Flurazepam

Product NDC

0143-3367

11-digit product format

001433367

Labeler code

0143

Product ID

0143-3367_3897b6f0-5a9e-4ea1-8f4e-c8cc47547d19

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Flurazepam Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

West-ward Pharmaceutical Corp

Application

ANDA077107

Marketing category

ANDA

Marketing start

1986-12-08

Marketing end

0000-00-00

Substance

FLURAZEPAM HYDROCHLORIDE

Active strength

15 mg/1

Pharmacologic classes

Benzodiazepine [EPC],Benzodiazepines [CS]

DEA schedule

CIV

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record