Methylphenidate Hydrochloride

Product NDC
63629-3166
11-digit product format
636293166
Labeler code
63629
Product ID
63629-3166_dc53c683-725e-4e46-bed4-89ab26b787ca
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
methylphenidate hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
NDA010187
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
1955-12-31
Marketing end
0000-00-00
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
2021-12-31
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
63629-3166-1EA - Each63629-316687449206-839a-48b2-9c6d-ed5e2186b23c12012-07-24
63629-3166-2EA - Each63629-316653f23d45-9b5f-44b0-bab5-2294e0c26b2c12012-07-24
63629-3166-3EA - Each63629-3166edac12b6-340a-4447-8aae-b7fb26ed57d212012-07-24
63629-3166-4EA - Each63629-3166c6be36b8-098c-4899-86a6-a538b557309d12012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-3166-16362931660130 TABLET in 1 BOTTLE (63629-3166-1) 30 tablet2011-01-270000-00-00NoNoCurrent
63629-3166-263629316602100 TABLET in 1 BOTTLE (63629-3166-2) 100 tablet2011-01-270000-00-00NoNoCurrent
63629-3166-36362931660390 TABLET in 1 BOTTLE (63629-3166-3) 90 tablet2011-01-270000-00-00NoNoCurrent
63629-3166-46362931660460 TABLET in 1 BOTTLE (63629-3166-4) 60 tablet2011-01-270000-00-00NoNoCurrent