Active Ingredient: SUCCINYLCHOLINE CHLORIDE
Proprietary Name: SUCCINYLCHOLINE CHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 20MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A213552
Product Number: 001
Approval Date: Oct 27, 2020
Applicant Holder Full Name: NEXUS PHARMACEUTICALS LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
