Active Ingredient: ZINC CHLORIDE
Proprietary Name: ZINC CHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1MG ZINC/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A216152
Product Number: 001
Approval Date: Oct 16, 2024
Applicant Holder Full Name: SOMERSET THERAPEUTICS LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
