Dexmethylphenidate hydrochloride

Product NDC
63629-1098
11-digit product format
636291098
Labeler code
63629
Product ID
63629-1098_b4053bd8-6d5b-4d57-b0a8-8a901a3cebe2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Dexmethylphenidate hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA201231
Marketing category
ANDA
Marketing start
2020-06-17
Marketing end
0000-00-00
Substance
DEXMETHYLPHENIDATE HYDROCHLORIDE
Active strength
10 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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63629-1098-1EA - Each63629-1098682f445a-c228-4922-91ab-89b3384e747512020-09-14