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Risperidone - 60505-2587-7 - (Risperidone)

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Drug Information of Risperidone

Product NDC: 60505-2587
Proprietary Name: Risperidone
Non Proprietary Name: Risperidone
Active Ingredient(s): 2    mg/1 & nbsp;   Risperidone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Risperidone

Product NDC: 60505-2587
Labeler Name: Apotex Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077953
Marketing Category: ANDA
Start Marketing Date: 20080922

Package Information of Risperidone

Package NDC: 60505-2587-7
Package Description: 10000 TABLET in 1 BOTTLE (60505-2587-7)

NDC Information of Risperidone

NDC Code 60505-2587-7
Proprietary Name Risperidone
Package Description 10000 TABLET in 1 BOTTLE (60505-2587-7)
Product NDC 60505-2587
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Risperidone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080922
Marketing Category Name ANDA
Labeler Name Apotex Corp
Substance Name RISPERIDONE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Risperidone


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