Alprazolam

Product NDC

21695-248

11-digit product format

216950248

Labeler code

21695

Product ID

21695-248_4f300492-4080-499d-b872-a8bf9de3cc7c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Alprazolam

Dosage form

TABLET

Route

ORAL

Labeler

Rebel Distributors Corp.

Application

ANDA074112

Marketing category

ANDA

Marketing start

1999-12-29

Marketing end

0000-00-00

Substance

ALPRAZOLAM

Active strength

1 mg/1

Pharmacologic classes

Benzodiazepine [EPC],Benzodiazepines [CS]

DEA schedule

CIV

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record