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Active Ingredient: DIFLUNISAL
Proprietary Name: DIFLUNISAL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 500MG
Reference Listed Drug: No
Reference Standard: No
TE Code: Application Number: A074604
Product Number: 001
Approval Date: Jun 10, 1996
Applicant Holder Full Name: ANI PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information