FDA Drug Application (078690) for CARBIDOPA AND LEVODOPA by SUN PHARMA GLOBAL

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Application Number078690
Product Number001
FormTABLET, ORALLY DISINTEGRATING;ORAL
Dosage10MG;100MG
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameCARBIDOPA AND LEVODOPA
Active IngredientCARBIDOPA; LEVODOPA

Active IngredientCount
List of drugs with Active Ingredient CARBIDOPA16
List of drugs with Active Ingredient LEVODOPA17


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