METHYLPHENIDATE HYDROCHLORIDE

Product NDC
64720-239
11-digit product format
647200239
Labeler code
64720
Product ID
64720-239_0586bffb-ae48-4a5d-876c-b0fb62d7802f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
METHYLPHENIDATE HYDROCHLORIDE
Dosage form
TABLET
Route
ORAL
Labeler
CorePharma, LLC
Application
ANDA091159
Marketing category
ANDA
Marketing start
2014-04-07
Marketing end
2019-06-30
Substance
METHYLPHENIDATE HYDROCHLORIDE
Active strength
20 mg/1
Pharmacologic classes
Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]
DEA schedule
CII
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
64720-239-10EA - Each64720-2391005fef4-f65c-41dd-9a19-419ed6911d3912014-05-02