Risperidone

Product NDC
64679-571
11-digit product format
646790571
Labeler code
64679
Product ID
64679-571_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
3 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
64679-571-02EA - Each64679-5710aea97bd-112f-491e-a04c-2a99030f053a12012-07-24
64679-571-04EA - Each64679-571c519edaf-e762-4a34-b7e9-77836f6706da12012-07-24