Ibuprofen

Product NDC
50090-2463
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA091239
Marketing category
ANDA
Substance
IBUPROFEN
Current FDA listing
Historical FDA.report record

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-2463-050 TABLET in 1 BOTTLE (50090-2463-0) 2016-09-120000-00-00NoCurrent
50090-2463-220 TABLET in 1 BOTTLE (50090-2463-2) 2016-10-060000-00-00NoCurrent
50090-2463-324 TABLET in 1 BOTTLE (50090-2463-3) 2016-09-060000-00-00NoCurrent
50090-2463-440 TABLET in 1 BOTTLE (50090-2463-4) 2016-10-060000-00-00NoCurrent
50090-2463-530 TABLET in 1 BOTTLE (50090-2463-5) 2016-10-100000-00-00NoCurrent
50090-2463-628 TABLET in 1 BOTTLE (50090-2463-6) 2017-01-040000-00-00NoCurrent
50090-2463-760 TABLET in 1 BOTTLE (50090-2463-7) 2016-09-200000-00-00NoCurrent
50090-2463-8100 TABLET in 1 BOTTLE (50090-2463-8) 2016-12-140000-00-00NoCurrent

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Drug FactsA-S Medication Solutions2019-04-25HUMAN OTC DRUG LABEL1