RISPERDAL - 21695-115-60 - (risperidone)

Alphabetical Index


Drug Information of RISPERDAL

Product NDC: 21695-115
Proprietary Name: RISPERDAL
Non Proprietary Name: risperidone
Active Ingredient(s): 3    mg/1 & nbsp;   risperidone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of RISPERDAL

Product NDC: 21695-115
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020272
Marketing Category: NDA
Start Marketing Date: 19931229

Package Information of RISPERDAL

Package NDC: 21695-115-60
Package Description: 60 TABLET in 1 BOTTLE (21695-115-60)

NDC Information of RISPERDAL

NDC Code 21695-115-60
Proprietary Name RISPERDAL
Package Description 60 TABLET in 1 BOTTLE (21695-115-60)
Product NDC 21695-115
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 Rebel Distributors Corp
Substance Name RISPERIDONE
Strength Number 3
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of RISPERDAL


General Information