Alprazolam

Product NDC

68788-6865

11-digit product format

687886865

Labeler code

68788

Product ID

68788-6865_47ccf9d6-0126-422c-9695-b1e7ae974f50

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Alprazolam

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA200739

Marketing category

ANDA

Marketing start

2017-01-10

Marketing end

0000-00-00

Substance

ALPRAZOLAM

Active strength

0 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