Ibuprofen - 63629-1469-0 - (Ibuprofen)

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Drug Information of Ibuprofen

Product NDC: 63629-1469
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: 63629-1469
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078558
Marketing Category: ANDA
Start Marketing Date: 20091123

Package Information of Ibuprofen

Package NDC: 63629-1469-0
Package Description: 21 TABLET in 1 BOTTLE (63629-1469-0)

NDC Information of Ibuprofen

NDC Code 63629-1469-0
Proprietary Name Ibuprofen
Package Description 21 TABLET in 1 BOTTLE (63629-1469-0)
Product NDC 63629-1469
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 Bryant Ranch Prepack
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