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Perrigo Ibuprofen - 10768-7167-2 - (ibuprofen)

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Drug Information of Perrigo Ibuprofen

Product NDC: 10768-7167
Proprietary Name: Perrigo 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 Perrigo Ibuprofen

Product NDC: 10768-7167
Labeler Name: Perrigo Pharmaceuticals Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077114
Marketing Category: ANDA
Start Marketing Date: 20060316

Package Information of Perrigo Ibuprofen

Package NDC: 10768-7167-2
Package Description: 500 TABLET in 1 BOTTLE (10768-7167-2)

NDC Information of Perrigo Ibuprofen

NDC Code 10768-7167-2
Proprietary Name Perrigo Ibuprofen
Package Description 500 TABLET in 1 BOTTLE (10768-7167-2)
Product NDC 10768-7167
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060316
Marketing Category Name ANDA
Labeler Name Perrigo Pharmaceuticals Company
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 Perrigo Ibuprofen


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