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Active Ingredient: METHYLPREDNISOLONE
Proprietary Name: METHYLPREDNISOLONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 4MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A040194
Product Number: 001
Approval Date: Oct 31, 1997
Applicant Holder Full Name: SANDOZ INC
Marketing Status:
Prescription
Patent and Exclusivity Information
