RISPERDAL - 55289-465-30 - (risperidone)

Alphabetical Index


Drug Information of RISPERDAL

Product NDC: 55289-465
Proprietary Name: RISPERDAL
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 RISPERDAL

Product NDC: 55289-465
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020272
Marketing Category: NDA
Start Marketing Date: 19931229

Package Information of RISPERDAL

Package NDC: 55289-465-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (55289-465-30)

NDC Information of RISPERDAL

NDC Code 55289-465-30
Proprietary Name RISPERDAL
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (55289-465-30)
Product NDC 55289-465
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 PD-Rx Pharmaceuticals, Inc.
Substance Name RISPERIDONE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of RISPERDAL


General Information