Ibuprofen - 67046-309-30 - (Ibuprofen)

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Drug Information of Ibuprofen

Product NDC: 67046-309
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: 67046-309
Labeler Name: Contract Pharmacy Services-PA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075682
Marketing Category: ANDA
Start Marketing Date: 20090922

Package Information of Ibuprofen

Package NDC: 67046-309-30
Package Description: 30 TABLET in 1 BLISTER PACK (67046-309-30)

NDC Information of Ibuprofen

NDC Code 67046-309-30
Proprietary Name Ibuprofen
Package Description 30 TABLET in 1 BLISTER PACK (67046-309-30)
Product NDC 67046-309
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090922
Marketing Category Name ANDA
Labeler Name Contract Pharmacy Services-PA
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