Aripiprazole

Product NDC

70518-2475

11-digit product format

705182475

Labeler code

70518

Product ID

70518-2475_b2c10256-3f25-b04b-e053-2995a90adcb6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Aripiprazole

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA204838

Marketing category

ANDA

Marketing start

2019-12-09

Marketing end

0000-00-00

Substance

ARIPIPRAZOLE

Active strength

30 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record