Active Ingredient: CHROMIC CHLORIDE
Proprietary Name: CHROMIC CHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 0.004MG CHROMIUM/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N019271
Product Number: 001
Approval Date: May 5, 1987
Applicant Holder Full Name: ABRAXIS PHARMACEUTICAL PRODUCTS
Marketing Status:
Discontinued
Patent and Exclusivity Information