Active Ingredient: METHYLPREDNISOLONE SODIUM SUCCINATE
Proprietary Name: METHYLPREDNISOLONE SODIUM SUCCINATE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A087852
Product Number: 001
Approval Date: Feb 9, 1983
Applicant Holder Full Name: INTERNATIONAL MEDICATION SYSTEMS LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information
