Ibuprofen

Product NDC
37012-604
11-digit product format
370120604
Labeler code
37012
Product ID
37012-604_7375e2f1-691c-4321-87da-50380ee01428
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Shopko Stores Operating Co., LLC
Application
ANDA072096
Marketing category
ANDA
Marketing start
2013-09-09
Marketing end
0000-00-00
Substance
IBUPROFEN
Active strength
200 mg/1
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37012-604-71370120604711 BOTTLE in 1 CARTON (37012-604-71) > 50 TABLET, FILM COATED in 1 BOTTLE1 bottle2018-11-290000-00-00NoNoCurrent
37012-604-78370120604781 BOTTLE in 1 CARTON (37012-604-78) > 100 TABLET, FILM COATED in 1 BOTTLE1 bottle2013-09-090000-00-00NoNoCurrent
37012-604-85370120604851 BOTTLE in 1 CARTON (37012-604-85) > 250 TABLET, FILM COATED in 1 BOTTLE1 bottle2014-08-130000-00-00NoNoCurrent
37012-604-9037012060490500 TABLET, FILM COATED in 1 BOTTLE (37012-604-90) 2013-09-090000-00-00NoNoCurrent