Risperidone

Product NDC
64679-555
11-digit product format
646790555
Labeler code
64679
Product ID
64679-555_b3eefb63-0cd7-4733-b75a-1088cc99e115
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Risperidone
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Wockhardt USA LLC.
Application
ANDA078871
Marketing category
ANDA
Marketing start
2008-10-09
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

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
64679-555-02EA - Each64679-555211a85b9-a7c2-40fd-95d9-4cd9fead6af012012-07-24
64679-555-04EA - Each64679-5551bdf8095-b6d5-489d-996f-962aae4f0bfa12012-07-24