methylphenidate hydrochloride

Product NDC
68084-816
11-digit product format
680840816
Labeler code
68084
Product ID
68084-816_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
2020-08-31
Substance
METHYLPHENIDATE HYDROCHLORIDE
Active strength
27 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
68084-816-11EA - Each68084-816c0bfe265-c0d5-437b-9987-013d7cb2260512014-10-03
68084-816-21EA - Each68084-816e0ec7226-d4cd-4af6-888b-d436586afeba12014-10-03