Risperidone

Product NDC
65862-119
11-digit product format
658620119
Labeler code
65862
Product ID
65862-119_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
0 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
65862-119-05EA - Each65862-1190a572d5b-3407-4f6d-b602-f7719a939c4212012-07-24
65862-119-60EA - Each65862-1197e87c7ef-94f6-4ffb-8da0-26e3ea05cded12012-07-24