Ibuprofen - 25000-117-03 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 25000-117
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: 25000-117
Labeler Name: Marksans Pharma Limited
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA091239
Marketing Category: ANDA
Start Marketing Date: 20110725

Package Information of Ibuprofen

Package NDC: 25000-117-03
Package Description: 30 TABLET in 1 BOTTLE (25000-117-03)

NDC Information of Ibuprofen

NDC Code 25000-117-03
Proprietary Name Ibuprofen
Package Description 30 TABLET in 1 BOTTLE (25000-117-03)
Product NDC 25000-117
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110725
Marketing Category Name ANDA
Labeler Name Marksans Pharma Limited
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen


General Information