Ibuprofen - 25000-115-14 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 25000-115
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: 25000-115
Labeler Name: MARKSANS PHARMA LIMITED
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA091237
Marketing Category: ANDA
Start Marketing Date: 20120704

Package Information of Ibuprofen

Package NDC: 25000-115-14
Package Description: 1000 TABLET in 1 BOTTLE (25000-115-14)

NDC Information of Ibuprofen

NDC Code 25000-115-14
Proprietary Name Ibuprofen
Package Description 1000 TABLET in 1 BOTTLE (25000-115-14)
Product NDC 25000-115
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120704
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