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RISPERIDONE - 64679-555-03 - (RISPERIDONE)

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Drug Information of RISPERIDONE

Product NDC: 64679-555
Proprietary Name: RISPERIDONE
Non Proprietary Name: RISPERIDONE
Active Ingredient(s): 1    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: 64679-555
Labeler Name: WOCKHARDT USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078871
Marketing Category: ANDA
Start Marketing Date: 20081009

Package Information of RISPERIDONE

Package NDC: 64679-555-03
Package Description: 100 BLISTER PACK in 1 CARTON (64679-555-03) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of RISPERIDONE

NDC Code 64679-555-03
Proprietary Name RISPERIDONE
Package Description 100 BLISTER PACK in 1 CARTON (64679-555-03) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 64679-555
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name RISPERIDONE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20081009
Marketing Category Name ANDA
Labeler Name WOCKHARDT USA LLC
Substance Name RISPERIDONE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of RISPERIDONE


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