Flurazepam

Product NDC

68788-0408

11-digit product format

687880408

Labeler code

68788

Product ID

68788-0408_4bb22c6e-a74f-4a01-8e2a-e59eaa7369c7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Flurazepam Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc

Application

ANDA071108

Marketing category

ANDA

Marketing start

2012-01-27

Marketing end

0000-00-00

Substance

FLURAZEPAM HYDROCHLORIDE

Active strength

30 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