small molecule

HEXABRIX

IOXAGLATE MEGLUMINE; IOXAGLATE SODIUM

Loss of exclusivityloss of exclusivity
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Drug detail

Brand nameHEXABRIX
Active ingredientIOXAGLATE MEGLUMINE; IOXAGLATE SODIUM
Strength39.3%;19.6%
Dosage formINJECTABLE
RouteINJECTION
ModalitySmall molecule
FDA approvalJuly 1985
Marketing statusDISCN

Source: FDA Orange Book, layered on the CliffBio company graph. Cliff dates are the loss of exclusivity; estimates are projections, not legal advice.

HEXABRIX patent cliff — loss of exclusivity — | CliffBio