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risperidone - 68382-113-10 - (risperidone)

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Drug Information of risperidone

Product NDC: 68382-113
Proprietary Name: risperidone
Non Proprietary Name: risperidone
Active Ingredient(s): .5    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: 68382-113
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078040
Marketing Category: ANDA
Start Marketing Date: 20081113

Package Information of risperidone

Package NDC: 68382-113-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (68382-113-10)

NDC Information of risperidone

NDC Code 68382-113-10
Proprietary Name risperidone
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (68382-113-10)
Product NDC 68382-113
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name risperidone
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20081113
Marketing Category Name ANDA
Labeler Name Zydus Pharmaceuticals (USA) Inc.
Substance Name RISPERIDONE
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of risperidone


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