Alprazolam

Product NDC

68071-3049

11-digit product format

680713049

Labeler code

68071

Product ID

68071-3049_4a67b04d-4b46-5fe6-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Alprazolam

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA200739

Marketing category

ANDA

Marketing start

2015-10-01

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

2020-12-31

Current FDA listing

Historical FDA.report record