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risperidone - 49349-516-02 - (risperidone)

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Drug Information of risperidone

Product NDC: 49349-516
Proprietary Name: risperidone
Non Proprietary Name: risperidone
Active Ingredient(s): .25    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: 49349-516
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078040
Marketing Category: ANDA
Start Marketing Date: 20130501

Package Information of risperidone

Package NDC: 49349-516-02
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (49349-516-02)

NDC Information of risperidone

NDC Code 49349-516-02
Proprietary Name risperidone
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (49349-516-02)
Product NDC 49349-516
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name risperidone
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130501
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name RISPERIDONE
Strength Number .25
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of risperidone


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