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Risperidone - 50458-595-60 - (risperidone)

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Drug Information of Risperidone

Product NDC: 50458-595
Proprietary Name: Risperidone
Non Proprietary Name: risperidone
Active Ingredient(s): 4    mg/1 & nbsp;   risperidone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Risperidone

Product NDC: 50458-595
Labeler Name: Janssen Pharmaceutical, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020272
Marketing Category: NDA
Start Marketing Date: 19931229

Package Information of Risperidone

Package NDC: 50458-595-60
Package Description: 60 TABLET in 1 BOTTLE (50458-595-60)

NDC Information of Risperidone

NDC Code 50458-595-60
Proprietary Name Risperidone
Package Description 60 TABLET in 1 BOTTLE (50458-595-60)
Product NDC 50458-595
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name risperidone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19931229
Marketing Category Name NDA
Labeler Name Janssen Pharmaceutical, Inc.
Substance Name RISPERIDONE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Risperidone


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