Methylphenidate Hydrochloride (LA)

Product NDC
51862-267
11-digit product format
518620267
Labeler code
51862
Product ID
51862-267_5a7c9051-b72d-4c35-9fd5-b670fc00e7f5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methylphenidate Hydrochloride
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Labeler
Mayne Pharma
Application
ANDA078458
Marketing category
ANDA
Marketing start
2017-02-20
Marketing end
0000-00-00
Substance
METHYLPHENIDATE HYDROCHLORIDE
Active strength
60 mg/1
Pharmacologic classes
Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]
DEA schedule
CII
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51862-267-30EA - Each51862-267757930fd-40a6-4044-929d-5202cb515abc12017-03-06