IBUPROFEN - 16590-124-90 - (IBUPROFEN)

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Drug Information of IBUPROFEN

Product NDC: 16590-124
Proprietary Name: IBUPROFEN
Non Proprietary Name: IBUPROFEN
Active Ingredient(s): 400    mg/1 & nbsp;   IBUPROFEN
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of IBUPROFEN

Product NDC: 16590-124
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075682
Marketing Category: ANDA
Start Marketing Date: 20081120

Package Information of IBUPROFEN

Package NDC: 16590-124-90
Package Description: 90 TABLET in 1 BOTTLE (16590-124-90)

NDC Information of IBUPROFEN

NDC Code 16590-124-90
Proprietary Name IBUPROFEN
Package Description 90 TABLET in 1 BOTTLE (16590-124-90)
Product NDC 16590-124
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name IBUPROFEN
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20081120
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
Substance Name IBUPROFEN
Strength Number 400
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