Alprazolam

Product NDC

71335-0850

11-digit product format

713350850

Labeler code

71335

Product ID

71335-0850_f4b093f4-6ebd-41b7-8774-c21ee596fe64

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

1 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