Aripiprazole

Product NDC

70518-0765

11-digit product format

705180765

Labeler code

70518

Product ID

70518-0765_8e7dd4a9-463d-ff8a-e053-2995a90afab6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Aripiprazole

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA205064

Marketing category

ANDA

Marketing start

2017-10-06

Marketing end

0000-00-00

Substance

ARIPIPRAZOLE

Active strength

30 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record