Ibuprofen - 25000-123-03 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 25000-123
Proprietary Name: Ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 800    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen

Product NDC: 25000-123
Labeler Name: MARKSANS PHARMA LIMITED
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090796
Marketing Category: ANDA
Start Marketing Date: 20110228

Package Information of Ibuprofen

Package NDC: 25000-123-03
Package Description: 30 TABLET in 1 BOTTLE (25000-123-03)

NDC Information of Ibuprofen

NDC Code 25000-123-03
Proprietary Name Ibuprofen
Package Description 30 TABLET in 1 BOTTLE (25000-123-03)
Product NDC 25000-123
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110228
Marketing Category Name ANDA
Labeler Name MARKSANS PHARMA LIMITED
Substance Name IBUPROFEN
Strength Number 800
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Ibuprofen


General Information