ibuprofen - 55312-604-71 - (Ibuprofen)

Alphabetical Index


Drug Information of ibuprofen

Product NDC: 55312-604
Proprietary Name: ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 200    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of ibuprofen

Product NDC: 55312-604
Labeler Name: Western Family Foods Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA072096
Marketing Category: ANDA
Start Marketing Date: 20010905

Package Information of ibuprofen

Package NDC: 55312-604-71
Package Description: 1 BOTTLE in 1 CARTON (55312-604-71) > 50 TABLET in 1 BOTTLE

NDC Information of ibuprofen

NDC Code 55312-604-71
Proprietary Name ibuprofen
Package Description 1 BOTTLE in 1 CARTON (55312-604-71) > 50 TABLET in 1 BOTTLE
Product NDC 55312-604
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20010905
Marketing Category Name ANDA
Labeler Name Western Family Foods Inc
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of ibuprofen


General Information