FDA Drug Application (020707) for SKELID by SANOFI AVENTIS US

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Application Number020707
Product Number001
FormTABLET;ORAL
DosageEQ 200MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameSKELID
Active IngredientTILUDRONATE DISODIUM



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