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Active Ingredient: OXAPROZIN
Proprietary Name: OXAPROZIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 600MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A075845
Product Number: 001
Approval Date: Jan 31, 2001
Applicant Holder Full Name: SANDOZ INC
Marketing Status:
Prescription
Patent and Exclusivity Information