Risperidone

Product NDC
65862-121
11-digit product format
658620121
Labeler code
65862
Product ID
65862-121_5d2750a4-025a-40a1-97d2-d9447a37afbb
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Risperidone
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Aurobindo Pharma Limited
Application
ANDA078269
Marketing category
ANDA
Marketing start
2008-10-08
Marketing end
0000-00-00
Substance
RISPERIDONE
Active strength
1 mg/1
Pharmacologic classes
Atypical Antipsychotic [EPC]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
65862-121-05EA - Each65862-12135c9b041-cd52-4bc1-882e-785e2c23aabc12012-07-24
65862-121-60EA - Each65862-1214a145a02-e933-42be-a2d7-623bc1a5725c12012-07-24