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

Active IngredientCount
List of drugs with Active Ingredient DANTROLENE SODIUM4


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