Alprazolam

Product NDC

50436-4636

11-digit product format

504364636

Labeler code

50436

Product ID

50436-4636_89ce9063-c6e8-49e2-8a5e-bca74d628cc2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Alprazolam

Dosage form

TABLET

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA074112

Marketing category

ANDA

Marketing start

1995-12-29

Marketing end

0000-00-00

Substance

ALPRAZOLAM

Active strength

1 mg/1

Pharmacologic classes

Benzodiazepine [EPC],Benzodiazepines [CS]

DEA schedule

CIV

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record