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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: AP
Application Number: A216003
Product Number: 001
Approval Date: Feb 7, 2022
Applicant Holder Full Name: BE PHARMACEUTICALS AG
Marketing Status:
Prescription
Patent and Exclusivity Information
