Risperidone

Product NDC
64679-557
11-digit product format
646790557
Labeler code
64679
Product ID
64679-557_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
2 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
64679-557-02EA - Each64679-55701a6efcb-c74d-49af-91a6-7ad29c51f4ec12012-07-24
64679-557-04EA - Each64679-557f0829564-b494-483b-8750-b4759983e25612012-07-24