Oxaprozin - 21695-100-28 - (Oxaprozin)

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Drug Information of Oxaprozin

Product NDC: 21695-100
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: 21695-100
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075849
Marketing Category: ANDA
Start Marketing Date: 20100908

Package Information of Oxaprozin

Package NDC: 21695-100-28
Package Description: 28 TABLET, FILM COATED in 1 BOTTLE (21695-100-28)

NDC Information of Oxaprozin

NDC Code 21695-100-28
Proprietary Name Oxaprozin
Package Description 28 TABLET, FILM COATED in 1 BOTTLE (21695-100-28)
Product NDC 21695-100
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxaprozin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100908
Marketing Category Name ANDA
Labeler Name Rebel Distributors 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