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risperidone - 68382-155-06 - (risperidone)

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Drug Information of risperidone

Product NDC: 68382-155
Proprietary Name: risperidone
Non Proprietary Name: risperidone
Active Ingredient(s): 1    mg/1 & nbsp;   risperidone
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of risperidone

Product NDC: 68382-155
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078516
Marketing Category: ANDA
Start Marketing Date: 20100629

Package Information of risperidone

Package NDC: 68382-155-06
Package Description: 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68382-155-06)

NDC Information of risperidone

NDC Code 68382-155-06
Proprietary Name risperidone
Package Description 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68382-155-06)
Product NDC 68382-155
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name risperidone
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20100629
Marketing Category Name ANDA
Labeler Name Zydus Pharmaceuticals (USA) Inc.
Substance Name RISPERIDONE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of risperidone


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