FDA Drug Application (087835) for OXTRIPHYLLINE by WATSON LABS

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Application Number087835
Product Number001
FormTABLET, DELAYED RELEASE;ORAL
Dosage200MG
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameOXTRIPHYLLINE
Active IngredientOXTRIPHYLLINE

Active IngredientCount
List of drugs with Active Ingredient OXTRIPHYLLINE4


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