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RISPERIDONE - 64679-692-01 - (RISPERIDONE)

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Drug Information of RISPERIDONE

Product NDC: 64679-692
Proprietary Name: RISPERIDONE
Non Proprietary Name: RISPERIDONE
Active Ingredient(s): 1    mg/mL & nbsp;   RISPERIDONE
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of RISPERIDONE

Product NDC: 64679-692
Labeler Name: WOCKHARDT USA LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078744
Marketing Category: ANDA
Start Marketing Date: 20091014

Package Information of RISPERIDONE

Package NDC: 64679-692-01
Package Description: 30 mL in 1 BOTTLE (64679-692-01)

NDC Information of RISPERIDONE

NDC Code 64679-692-01
Proprietary Name RISPERIDONE
Package Description 30 mL in 1 BOTTLE (64679-692-01)
Product NDC 64679-692
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name RISPERIDONE
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20091014
Marketing Category Name ANDA
Labeler Name WOCKHARDT USA LLC.
Substance Name RISPERIDONE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of RISPERIDONE


General Information