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Risperidone - 62756-634-08 - (Risperidone)

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Drug Information of Risperidone

Product NDC: 62756-634
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: 62756-634
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078464
Marketing Category: ANDA
Start Marketing Date: 20130413

Package Information of Risperidone

Package NDC: 62756-634-08
Package Description: 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (62756-634-08)

NDC Information of Risperidone

NDC Code 62756-634-08
Proprietary Name Risperidone
Package Description 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (62756-634-08)
Product NDC 62756-634
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Risperidone
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20130413
Marketing Category Name ANDA
Labeler Name Sun Pharmaceutical Industries Limited
Substance Name RISPERIDONE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Risperidone


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