Alprazolam

Product NDC

71335-0422

11-digit product format

713350422

Labeler code

71335

Product ID

71335-0422_71576660-41ca-451a-922b-b385c8189760

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Alprazolam

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA074342

Marketing category

ANDA

Marketing start

1993-10-01

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