RISPERDAL - 50458-300-01 - (risperidone)

Alphabetical Index


Drug Information of RISPERDAL

Product NDC: 50458-300
Proprietary Name: RISPERDAL
Non Proprietary Name: risperidone
Active Ingredient(s): 1    mg/1 & nbsp;   risperidone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of RISPERDAL

Product NDC: 50458-300
Labeler Name: Janssen Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020272
Marketing Category: NDA
Start Marketing Date: 19931229

Package Information of RISPERDAL

Package NDC: 50458-300-01
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (50458-300-01) > 10 TABLET in 1 BLISTER PACK

NDC Information of RISPERDAL

NDC Code 50458-300-01
Proprietary Name RISPERDAL
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (50458-300-01) > 10 TABLET in 1 BLISTER PACK
Product NDC 50458-300
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name risperidone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19931229
Marketing Category Name NDA
Labeler Name Janssen Pharmaceuticals, Inc.
Substance Name RISPERIDONE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of RISPERDAL


General Information