Ibuprofen - 54569-4002-2 - (Ibuprofen)

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Drug Information of Ibuprofen

Product NDC: 54569-4002
Proprietary Name: Ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 600    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen

Product NDC: 54569-4002
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078558
Marketing Category: ANDA
Start Marketing Date: 20091123

Package Information of Ibuprofen

Package NDC: 54569-4002-2
Package Description: 4 TABLET in 1 BOTTLE (54569-4002-2)

NDC Information of Ibuprofen

NDC Code 54569-4002-2
Proprietary Name Ibuprofen
Package Description 4 TABLET in 1 BOTTLE (54569-4002-2)
Product NDC 54569-4002
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091123
Marketing Category Name ANDA
Labeler Name A-S Medication Solutions LLC
Substance Name IBUPROFEN
Strength Number 600
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