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Active Ingredient: TERIFLUNOMIDE
Proprietary Name: TERIFLUNOMIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 7MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A209677
Product Number: 002
Approval Date: Sep 28, 2023
Applicant Holder Full Name: SOLA PHARMACEUTICALS
Marketing Status:
Prescription
Patent and Exclusivity Information
Active Ingredient: TERIFLUNOMIDE
Proprietary Name: TERIFLUNOMIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 14MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A209677
Product Number: 001
Approval Date: Jun 17, 2020
Applicant Holder Full Name: SOLA PHARMACEUTICALS
Marketing Status:
Prescription
Patent and Exclusivity Information
