ibuprofen - 67877-296-05 - (ibuprofen)

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Drug Information of ibuprofen

Product NDC: 67877-296
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: 67877-296
Labeler Name: Ascend Laboratories, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090796
Marketing Category: ANDA
Start Marketing Date: 20120222

Package Information of ibuprofen

Package NDC: 67877-296-05
Package Description: 500 TABLET in 1 BOTTLE (67877-296-05)

NDC Information of ibuprofen

NDC Code 67877-296-05
Proprietary Name ibuprofen
Package Description 500 TABLET in 1 BOTTLE (67877-296-05)
Product NDC 67877-296
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120222
Marketing Category Name ANDA
Labeler Name Ascend Laboratories, LLC
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