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Risperidone - 59115-088-55 - (Risperidone)

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Drug Information of Risperidone

Product NDC: 59115-088
Proprietary Name: Risperidone
Non Proprietary Name: Risperidone
Active Ingredient(s): .25    mg/1 & nbsp;   Risperidone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Risperidone

Product NDC: 59115-088
Labeler Name: Hikma Pharmaceutical
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078740
Marketing Category: ANDA
Start Marketing Date: 20090601

Package Information of Risperidone

Package NDC: 59115-088-55
Package Description: 500 TABLET in 1 BOTTLE (59115-088-55)

NDC Information of Risperidone

NDC Code 59115-088-55
Proprietary Name Risperidone
Package Description 500 TABLET in 1 BOTTLE (59115-088-55)
Product NDC 59115-088
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Risperidone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090601
Marketing Category Name ANDA
Labeler Name Hikma Pharmaceutical
Substance Name RISPERIDONE
Strength Number .25
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Risperidone


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