Active Ingredient: ROFECOXIB
Proprietary Name: VIOXX
Dosage Form; Route of Administration: SUSPENSION; ORAL
Strength: 12.5MG/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N021052
Product Number: 001
Approval Date: May 20, 1999
Applicant Holder Full Name: MERCK RESEARCH LABORATORIES DIV MERCK CO INC
Marketing Status:
Discontinued
Patent and Exclusivity Information