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risperidone - 55154-1414-0 - (risperidone)

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Drug Information of risperidone

Product NDC: 55154-1414
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: 55154-1414
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020272
Marketing Category: NDA
Start Marketing Date: 19931229

Package Information of risperidone

Package NDC: 55154-1414-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-1414-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of risperidone

NDC Code 55154-1414-0
Proprietary Name risperidone
Package Description 10 BLISTER PACK in 1 BAG (55154-1414-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-1414
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 Cardinal Health
Substance Name RISPERIDONE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of risperidone


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