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Risperidone - 55154-6248-9 - (risperidone)

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Drug Information of Risperidone

Product NDC: 55154-6248
Proprietary Name: Risperidone
Non Proprietary Name: risperidone
Active Ingredient(s): 3    mg/1 & nbsp;   risperidone
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Risperidone

Product NDC: 55154-6248
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072688
Marketing Category: ANDA
Start Marketing Date: 20101112

Package Information of Risperidone

Package NDC: 55154-6248-9
Package Description: 6 BLISTER PACK in 1 CARTON (55154-6248-9) > 5 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Risperidone

NDC Code 55154-6248-9
Proprietary Name Risperidone
Package Description 6 BLISTER PACK in 1 CARTON (55154-6248-9) > 5 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-6248
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name risperidone
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101112
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name RISPERIDONE
Strength Number 3
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Risperidone


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