Active Ingredient: DANTROLENE SODIUM
Proprietary Name: DANTROLENE SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 20MG/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A205239
Product Number: 001
Approval Date: Feb 18, 2016
Applicant Holder Full Name: EUGIA PHARMA SPECIALITIES LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information
