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Risperidone - 13107-122-10 - (Risperidone)

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Drug Information of Risperidone

Product NDC: 13107-122
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: 13107-122
Labeler Name: Aurolife Pharma LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078269
Marketing Category: ANDA
Start Marketing Date: 20091025

Package Information of Risperidone

Package NDC: 13107-122-10
Package Description: 10 BLISTER PACK in 1 CARTON (13107-122-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Risperidone

NDC Code 13107-122-10
Proprietary Name Risperidone
Package Description 10 BLISTER PACK in 1 CARTON (13107-122-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 13107-122
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Risperidone
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20091025
Marketing Category Name ANDA
Labeler Name Aurolife Pharma LLC
Substance Name RISPERIDONE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Risperidone


General Information