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Risperidone - 59746-020-22 - (Risperidone)

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Drug Information of Risperidone

Product NDC: 59746-020
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: 59746-020
Labeler Name: Jubilant Cadista Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090839
Marketing Category: ANDA
Start Marketing Date: 20101201

Package Information of Risperidone

Package NDC: 59746-020-22
Package Description: 7 BLISTER PACK in 1 CARTON (59746-020-22) > 4 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Information of Risperidone

NDC Code 59746-020-22
Proprietary Name Risperidone
Package Description 7 BLISTER PACK in 1 CARTON (59746-020-22) > 4 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC 59746-020
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Risperidone
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20101201
Marketing Category Name ANDA
Labeler Name Jubilant Cadista Pharmaceuticals Inc.
Substance Name RISPERIDONE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Risperidone


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