Active Ingredient: METHYLPREDNISOLONE ACETATE
Proprietary Name: METHYLPREDNISOLONE ACETATE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 40MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A216502
Product Number: 001
Approval Date: Nov 3, 2023
Applicant Holder Full Name: AMNEAL EU LTD
Marketing Status:
Prescription
Patent and Exclusivity Information