Aripiprazole

Product NDC

70518-2149

11-digit product format

705182149

Labeler code

70518

Product ID

70518-2149_8c185666-ef20-4f54-e053-2a95a90a85ad

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Aripiprazole

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA202101

Marketing category

ANDA

Marketing start

2019-06-24

Marketing end

0000-00-00

Substance

ARIPIPRAZOLE

Active strength

15 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record