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Risperidone - 16252-562-60 - (Risperidone)

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Drug Information of Risperidone

Product NDC: 16252-562
Proprietary Name: Risperidone
Non Proprietary Name: Risperidone
Active Ingredient(s): 3    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: 16252-562
Labeler Name: Cobalt Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077860
Marketing Category: ANDA
Start Marketing Date: 20081205

Package Information of Risperidone

Package NDC: 16252-562-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (16252-562-60)

NDC Information of Risperidone

NDC Code 16252-562-60
Proprietary Name Risperidone
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (16252-562-60)
Product NDC 16252-562
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Risperidone
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20081205
Marketing Category Name ANDA
Labeler Name Cobalt Laboratories
Substance Name RISPERIDONE
Strength Number 3
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Risperidone


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