oxaprozin - 60505-0176-1 - (oxaprozin)

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Drug Information of oxaprozin

Product NDC: 60505-0176
Proprietary Name: oxaprozin
Non Proprietary Name: oxaprozin
Active Ingredient(s): 600    mg/1 & nbsp;   oxaprozin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of oxaprozin

Product NDC: 60505-0176
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075987
Marketing Category: ANDA
Start Marketing Date: 20040903

Package Information of oxaprozin

Package NDC: 60505-0176-1
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (60505-0176-1)

NDC Information of oxaprozin

NDC Code 60505-0176-1
Proprietary Name oxaprozin
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (60505-0176-1)
Product NDC 60505-0176
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxaprozin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20040903
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name OXAPROZIN
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 oxaprozin


General Information