RISPERDAL - 52125-294-02 - (risperidone)

Alphabetical Index


Drug Information of RISPERDAL

Product NDC: 52125-294
Proprietary Name: RISPERDAL
Non Proprietary Name: risperidone
Active Ingredient(s): .5    mg/1 & nbsp;   risperidone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of RISPERDAL

Product NDC: 52125-294
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020272
Marketing Category: NDA
Start Marketing Date: 20130507

Package Information of RISPERDAL

Package NDC: 52125-294-02
Package Description: 30 TABLET in 1 BLISTER PACK (52125-294-02)

NDC Information of RISPERDAL

NDC Code 52125-294-02
Proprietary Name RISPERDAL
Package Description 30 TABLET in 1 BLISTER PACK (52125-294-02)
Product NDC 52125-294
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name risperidone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130507
Marketing Category Name NDA
Labeler Name REMEDYREPACK INC.
Substance Name RISPERIDONE
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of RISPERDAL


General Information