Preferred Plus Ibuprofen

Product NDC

61715-057

11-digit product format

617150057

Labeler code

61715

Product ID

61715-057_28835a86-b0f8-400e-9c26-cd077955d640

Type

HUMAN OTC DRUG

Nonproprietary name

Ibuprofen

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Kinray, Inc.

Application

ANDA079129

Marketing category

ANDA

Marketing start

2013-05-11

Marketing end

0000-00-00

Substance

IBUPROFEN

Active strength

200 mg/1

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record