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Risperidone - 55154-3481-9 - (Risperidone)

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Drug Information of Risperidone

Product NDC: 55154-3481
Proprietary Name: Risperidone
Non Proprietary Name: Risperidone
Active Ingredient(s): 2    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: 55154-3481
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076879
Marketing Category: ANDA
Start Marketing Date: 20081024

Package Information of Risperidone

Package NDC: 55154-3481-9
Package Description: 6 BLISTER PACK in 1 CARTON (55154-3481-9) > 5 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Risperidone

NDC Code 55154-3481-9
Proprietary Name Risperidone
Package Description 6 BLISTER PACK in 1 CARTON (55154-3481-9) > 5 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-3481
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Risperidone
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20081024
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name RISPERIDONE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Risperidone


General Information