Alprazolam

Product NDC

71335-0448

11-digit product format

713350448

Labeler code

71335

Product ID

71335-0448_14d82b8a-1bb2-4550-9c25-1a82a2f108a6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Alprazolam

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA200739

Marketing category

ANDA

Marketing start

2015-10-01

Marketing end

0000-00-00

Substance

ALPRAZOLAM

Active strength

2 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