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RISPERIDONE - 16590-641-90 - (RISPERIDONE)

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Drug Information of RISPERIDONE

Product NDC: 16590-641
Proprietary Name: RISPERIDONE
Non Proprietary Name: RISPERIDONE
Active Ingredient(s): 2    mg/1 & nbsp;   RISPERIDONE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of RISPERIDONE

Product NDC: 16590-641
Labeler Name: STAT Rx USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079088
Marketing Category: ANDA
Start Marketing Date: 20090101

Package Information of RISPERIDONE

Package NDC: 16590-641-90
Package Description: 90 TABLET in 1 BOTTLE (16590-641-90)

NDC Information of RISPERIDONE

NDC Code 16590-641-90
Proprietary Name RISPERIDONE
Package Description 90 TABLET in 1 BOTTLE (16590-641-90)
Product NDC 16590-641
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name RISPERIDONE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090101
Marketing Category Name ANDA
Labeler Name STAT Rx USA LLC
Substance Name RISPERIDONE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of RISPERIDONE


General Information