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: AP
Application Number: A204762
Product Number: 001
Approval Date: Jun 19, 2017
Applicant Holder Full Name: HIKMA PHARMACEUTICALS LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
