FDA Drug Application (076686) for DANTROLENE SODIUM by ELITE LABS INC

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Application Number076686
Product Number001
FormCAPSULE;ORAL
Dosage25MG
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameDANTROLENE SODIUM
Active IngredientDANTROLENE SODIUM



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