Active Ingredient: METHYLPREDNISOLONE SODIUM SUCCINATE
Proprietary Name: METHYLPREDNISOLONE SODIUM SUCCINATE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 500MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A089186
Product Number: 001
Approval Date: Mar 28, 1986
Applicant Holder Full Name: ABRAXIS PHARMACEUTICAL PRODUCTS
Marketing Status:
Discontinued
Patent and Exclusivity Information
