Home > National Drug Code (NDC) > Risperidone

Risperidone - 67046-641-30 - (Risperidone)

Alphabetical Index


Drug Information of Risperidone

Product NDC: 67046-641
Proprietary Name: Risperidone
Non Proprietary Name: Risperidone
Active Ingredient(s): .5    mg/1 & nbsp;   Risperidone
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Risperidone

Product NDC: 67046-641
Labeler Name: Contract Pharmacy Services-PA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076228
Marketing Category: ANDA
Start Marketing Date: 20101206

Package Information of Risperidone

Package NDC: 67046-641-30
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-641-30)

NDC Information of Risperidone

NDC Code 67046-641-30
Proprietary Name Risperidone
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-641-30)
Product NDC 67046-641
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Risperidone
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101206
Marketing Category Name ANDA
Labeler Name Contract Pharmacy Services-PA
Substance Name RISPERIDONE
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Risperidone


General Information