Daypro

Daypro is a brand name of oxaprozin, approved by the FDA in the following formulation(s):

DAYPRO (oxaprozin - tablet; oral)

• 
  Manufacturer: GD SEARLE
  
  Approval date: October 29, 1992
  
  Strength(s): 600MG ^[RLD][AB]

Has a generic version of Daypro been approved?

Yes. The following products are equivalent to Daypro:

oxaprozin tablet; oral

• 
  Manufacturer: APOTEX INC
  
  Approval date: September 2, 2004
  
  Strength(s): 600MG ^[AB]


• 
  Manufacturer: CARACO
  
  Approval date: January 3, 2002
  
  Strength(s): 600MG ^[AB]


• 
  Manufacturer: DR REDDYS LABS LTD
  
  Approval date: January 31, 2001
  
  Strength(s): 600MG ^[AB]


• 
  Manufacturer: IVAX SUB TEVA PHARMS
  
  Approval date: May 13, 2002
  
  Strength(s): 600MG ^[AB]


• 
  Manufacturer: MYLAN
  
  Approval date: February 28, 2001
  
  Strength(s): 600MG ^[AB]


• 
  Manufacturer: SANDOZ
  
  Approval date: January 31, 2001
  
  Strength(s): 600MG ^[AB]


• 
  Manufacturer: TEVA
  
  Approval date: July 3, 2002
  
  Strength(s): 600MG ^[AB]


• 
  Manufacturer: WATSON LABS
  
  Approval date: February 9, 2001
  
  Strength(s): 600MG ^[AB]

Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Daypro. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.

Related Patents

There are no current U.S. patents associated with Daypro.

See also...

• Daypro Consumer Information (Wolters Kluwer)
• Daypro Consumer Information (Cerner Multum)
• Daypro Advanced Consumer Information (Micromedex)
• Oxaprozin Consumer Information (Wolters Kluwer)
• Oxaprozin Consumer Information (Cerner Multum)
• Oxaprozin Advanced Consumer Information (Micromedex)
• Oxaprozin AHFS DI Monographs (ASHP)
• Oxaprozin Potassium AHFS DI Monographs (ASHP)