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Risperidone - 0781-5314-08 - (Risperidone)

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Drug Information of Risperidone

Product NDC: 0781-5314
Proprietary Name: Risperidone
Non Proprietary Name: Risperidone
Active Ingredient(s): 4    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: 0781-5314
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078116
Marketing Category: ANDA
Start Marketing Date: 20091222

Package Information of Risperidone

Package NDC: 0781-5314-08
Package Description: 28 TABLET, ORALLY DISINTEGRATING in 1 CARTON (0781-5314-08)

NDC Information of Risperidone

NDC Code 0781-5314-08
Proprietary Name Risperidone
Package Description 28 TABLET, ORALLY DISINTEGRATING in 1 CARTON (0781-5314-08)
Product NDC 0781-5314
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Risperidone
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20091222
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name RISPERIDONE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Risperidone


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