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Risperidone - 49349-150-02 - (Risperidone)

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Drug Information of Risperidone

Product NDC: 49349-150
Proprietary Name: Risperidone
Non Proprietary Name: Risperidone
Active Ingredient(s): .5    mg/1 & nbsp;   Risperidone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Risperidone

Product NDC: 49349-150
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076879
Marketing Category: ANDA
Start Marketing Date: 20110411

Package Information of Risperidone

Package NDC: 49349-150-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-150-02)

NDC Information of Risperidone

NDC Code 49349-150-02
Proprietary Name Risperidone
Package Description 30 TABLET in 1 BLISTER PACK (49349-150-02)
Product NDC 49349-150
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Risperidone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110411
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name RISPERIDONE
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Risperidone


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