Daypro - 55289-453-20 - (oxaprozin)

Alphabetical Index


Drug Information of Daypro

Product NDC: 55289-453
Proprietary Name: Daypro
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 Daypro

Product NDC: 55289-453
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018841
Marketing Category: NDA
Start Marketing Date: 19921029

Package Information of Daypro

Package NDC: 55289-453-20
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-453-20)

NDC Information of Daypro

NDC Code 55289-453-20
Proprietary Name Daypro
Package Description 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-453-20)
Product NDC 55289-453
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxaprozin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19921029
Marketing Category Name NDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
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 Daypro


General Information