Aripiprazole

Product NDC

70518-1794

11-digit product format

705181794

Labeler code

70518

Product ID

70518-1794_969387cb-80fb-2db0-e053-2995a90ad33d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Aripiprazole

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA202101

Marketing category

ANDA

Marketing start

2019-01-11

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