IBUPROFEN

Product NDC

61786-948

11-digit product format

617860948

Labeler code

61786

Product ID

61786-948_5fa240c5-0a12-45a9-e053-2a91aa0a4ae8

Type

HUMAN OTC DRUG

Nonproprietary name

IBUPROFEN

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA091239

Marketing category

ANDA

Marketing start

2016-10-19

Marketing end

0000-00-00

Substance

IBUPROFEN

Active strength

200 mg/1

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record