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: A211625
Product Number: 001
Approval Date: May 19, 2020
Applicant Holder Full Name: UMEDICA LABORATORIES PRIVATE LTD
Marketing Status:
Prescription
Patent and Exclusivity Information