FDA Drug Application (017669) for TENUATE by SANOFI AVENTIS US

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Application Number017669
Product Number001
FormTABLET, EXTENDED RELEASE;ORAL
Dosage75MG
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameTENUATE
Active IngredientDIETHYLPROPION HYDROCHLORIDE

Active IngredientCount
List of drugs with Active Ingredient DIETHYLPROPION HYDROCHLORIDE5


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