Aripiprazole

Product NDC

0093-7582

11-digit product format

000937582

Labeler code

0093

Product ID

0093-7582_858b23a3-f76c-4ce9-b531-51d97c18c245

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Aripiprazole

Dosage form

TABLET

Route

ORAL

Labeler

Teva Pharmaceuticals USA, Inc.

Application

ANDA078708

Marketing category

ANDA

Marketing start

2015-04-28

Marketing end

2020-01-31

Substance

ARIPIPRAZOLE

Active strength

20 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record