Active Ingredient: SODIUM PHOSPHATE P-32
Proprietary Name: PHOSPHOTOPE
Dosage Form; Route of Administration: SOLUTION; INJECTION, ORAL
Strength: 1-8mCi/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N010927
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: BRACCO DIAGNOSTICS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
