Active Ingredient: PREDNISOLONE SODIUM PHOSPHATE
Proprietary Name: HYDELTRASOL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 20MG PHOSPHATE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N011583
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: MERCK AND CO INC
Marketing Status:
Discontinued
Patent and Exclusivity Information