Oxaprozin - 55111-170-01 - (Oxaprozin)

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Drug Information of Oxaprozin

Product NDC: 55111-170
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: 55111-170
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075855
Marketing Category: ANDA
Start Marketing Date: 20010131

Package Information of Oxaprozin

Package NDC: 55111-170-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (55111-170-01)

NDC Information of Oxaprozin

NDC Code 55111-170-01
Proprietary Name Oxaprozin
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (55111-170-01)
Product NDC 55111-170
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxaprozin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20010131
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
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