Ibuprofen - 42291-338-50 - (Ibuprofen)

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Drug Information of Ibuprofen

Product NDC: 42291-338
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: 42291-338
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078558
Marketing Category: ANDA
Start Marketing Date: 20130110

Package Information of Ibuprofen

Package NDC: 42291-338-50
Package Description: 500 TABLET in 1 BOTTLE (42291-338-50)

NDC Information of Ibuprofen

NDC Code 42291-338-50
Proprietary Name Ibuprofen
Package Description 500 TABLET in 1 BOTTLE (42291-338-50)
Product NDC 42291-338
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130110
Marketing Category Name ANDA
Labeler Name AvKARE, Inc.
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