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Risperidone - 0378-3512-91 - (risperidone)

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Drug Information of Risperidone

Product NDC: 0378-3512
Proprietary Name: Risperidone
Non Proprietary Name: risperidone
Active Ingredient(s): 2    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: 0378-3512
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076288
Marketing Category: ANDA
Start Marketing Date: 20080917

Package Information of Risperidone

Package NDC: 0378-3512-91
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3512-91)

NDC Information of Risperidone

NDC Code 0378-3512-91
Proprietary Name Risperidone
Package Description 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3512-91)
Product NDC 0378-3512
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name risperidone
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080917
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name RISPERIDONE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Risperidone


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