Alprazolam

Product NDC

68788-7588

11-digit product format

687887588

Labeler code

68788

Product ID

68788-7588_2459ddd5-c9ad-4517-bc97-b91126b5d531

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Alprazolam

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA074342

Marketing category

ANDA

Marketing start

1993-10-01

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

2021-12-31

Current FDA listing

Historical FDA.report record