ibuprofen - 0363-0604-52 - (Ibuprofen)

Alphabetical Index


Drug Information of ibuprofen

Product NDC: 0363-0604
Proprietary Name: ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 200    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ibuprofen

Product NDC: 0363-0604
Labeler Name: Walgreen Company
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA072096
Marketing Category: ANDA
Start Marketing Date: 20090121

Package Information of ibuprofen

Package NDC: 0363-0604-52
Package Description: 10 TABLET, FILM COATED in 1 BOTTLE (0363-0604-52)

NDC Information of ibuprofen

NDC Code 0363-0604-52
Proprietary Name ibuprofen
Package Description 10 TABLET, FILM COATED in 1 BOTTLE (0363-0604-52)
Product NDC 0363-0604
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090121
Marketing Category Name ANDA
Labeler Name Walgreen Company
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of ibuprofen


General Information