Ibuprofen

Product NDC

69256-199

11-digit product format

692560199

Labeler code

69256

Product ID

69256-199_fe8a391c-3cc3-4d16-a3b2-271d848f3459

Type

HUMAN OTC DRUG

Nonproprietary name

IBUPROFEN

Dosage form

CAPSULE, LIQUID FILLED

Route

ORAL

Labeler

Harris Teeter, LLC

Application

ANDA078682

Marketing category

ANDA

Marketing start

2015-02-28

Marketing end

2020-12-31

Substance

IBUPROFEN

Active strength

200 mg/1

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record