Active Ingredient: CHLORMERODRIN HG-197
Proprietary Name: CHLORMERODRIN HG 197
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 0.6-1.4mCi/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N017269
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
