Alprazolam

Product NDC

63739-669

11-digit product format

637390669

Labeler code

63739

Product ID

63739-669_b86ef043-5930-4eeb-b63a-b0af1844d0de

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Alprazolam

Dosage form

TABLET

Route

ORAL

Labeler

McKesson Corporation dba SKY Packaging

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