Up and Up Ibuprofen Sodium

Product NDC

11673-835

11-digit product format

116730835

Labeler code

11673

Product ID

11673-835_706e52e2-cd68-42f2-be61-42ac313889cf

Type

HUMAN OTC DRUG

Nonproprietary name

Ibuprofen

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Target Corporation

Application

ANDA206581

Marketing category

ANDA

Marketing start

2017-03-02

Marketing end

0000-00-00

Substance

IBUPROFEN SODIUM

Active strength

256 mg/1

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record