methylphenidate hydrochloride

Product NDC
68084-833
11-digit product format
680840833
Labeler code
68084
Product ID
68084-833_951f9025-3dc9-8e0b-e053-2a95a90ac51a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
methylphenidate hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
American Health Packaging
Application
NDA021121
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
2014-08-21
Marketing end
2020-09-30
Substance
METHYLPHENIDATE HYDROCHLORIDE
Active strength
54 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
68084-833-25EA - Each68084-833bea02a46-1fb6-4227-be85-40b0c8534d3912014-10-03
68084-833-95EA - Each68084-833fde6e2da-b745-40e9-ae1a-caf19347ab7e12014-10-03