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Risperidone - 0615-7508-39 - (risperidone)

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Drug Information of Risperidone

Product NDC: 0615-7508
Proprietary Name: Risperidone
Non Proprietary Name: risperidone
Active Ingredient(s): 4    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: 0615-7508
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072688
Marketing Category: ANDA
Start Marketing Date: 20100407

Package Information of Risperidone

Package NDC: 0615-7508-39
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-7508-39)

NDC Information of Risperidone

NDC Code 0615-7508-39
Proprietary Name Risperidone
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-7508-39)
Product NDC 0615-7508
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name risperidone
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100407
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name RISPERIDONE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Risperidone


General Information