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RISPERIDONE - 51991-320-01 - (RISPERIDONE)

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Drug Information of RISPERIDONE

Product NDC: 51991-320
Proprietary Name: RISPERIDONE
Non Proprietary Name: RISPERIDONE
Active Ingredient(s): 3    mg/1 & nbsp;   RISPERIDONE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of RISPERIDONE

Product NDC: 51991-320
Labeler Name: Breckenridge Pharmaceutical, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201003
Marketing Category: ANDA
Start Marketing Date: 20120425

Package Information of RISPERIDONE

Package NDC: 51991-320-01
Package Description: 100 TABLET in 1 BOTTLE (51991-320-01)

NDC Information of RISPERIDONE

NDC Code 51991-320-01
Proprietary Name RISPERIDONE
Package Description 100 TABLET in 1 BOTTLE (51991-320-01)
Product NDC 51991-320
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name RISPERIDONE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120425
Marketing Category Name ANDA
Labeler Name Breckenridge Pharmaceutical, Inc.
Substance Name RISPERIDONE
Strength Number 3
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of RISPERIDONE


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