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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 018905

HEXABRIX (IOXAGLATE MEGLUMINE; IOXAGLATE SODIUM)
39.3%;19.6%
Marketing Status: Discontinued
Active Ingredient: IOXAGLATE MEGLUMINE; IOXAGLATE SODIUM
Proprietary Name: HEXABRIX
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 39.3%;19.6%
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018905
Product Number: 002
Approval Date: Jul 26, 1985
Applicant Holder Full Name: GUERBET LLC
Marketing Status:  Discontinued
Patent and Exclusivity Information
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