Alprazolam

Product NDC

68788-9727

11-digit product format

687889727

Labeler code

68788

Product ID

68788-9727_c17d4f1b-03df-4f7a-9ce1-dc534cea6862

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Alprazolam

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA078387

Marketing category

ANDA

Marketing start

2012-11-15

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