Aripiprazole

Product NDC

70518-1624

11-digit product format

705181624

Labeler code

70518

Product ID

70518-1624_9567ac90-8861-4090-e053-2a95a90a21f8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Aripiprazole

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA204838

Marketing category

ANDA

Marketing start

2018-11-01

Marketing end

0000-00-00

Substance

ARIPIPRAZOLE

Active strength

20 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record