Ibuprofen - 67046-312-30 - (Ibuprofen)

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Drug Information of Ibuprofen

Product NDC: 67046-312
Proprietary Name: Ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 800    1/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen

Product NDC: 67046-312
Labeler Name: Contract Pharmacy Services-PA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075682
Marketing Category: ANDA
Start Marketing Date: 20100414

Package Information of Ibuprofen

Package NDC: 67046-312-30
Package Description: 30 TABLET in 1 BLISTER PACK (67046-312-30)

NDC Information of Ibuprofen

NDC Code 67046-312-30
Proprietary Name Ibuprofen
Package Description 30 TABLET in 1 BLISTER PACK (67046-312-30)
Product NDC 67046-312
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100414
Marketing Category Name ANDA
Labeler Name Contract Pharmacy Services-PA
Substance Name IBUPROFEN
Strength Number 800
Strength Unit 1/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Ibuprofen


General Information