Active Ingredient: SODIUM CHROMATE CR-51
Proprietary Name: CHROMITOPE SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 2mCi/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N013993
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: BRACCO DIAGNOSTICS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information