NDCFind

Methylphenidate Hydrochloride 62037-0734-01

Package NDC

62037-0734-01

Product NDC: 62037-0734

Manufacturer
Actavis Pharma, Inc.
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Product Type
Human Prescription Drug
DEA Schedule
Schedule CII
Marketing Start
March 4, 2019
Listing Expires
December 31, 2027
Application
ANDA076772

Active Ingredients

IngredientStrength
Methylphenidate Hydrochloride27 mg/1

Drug Class

Central Nervous System Stimulant [EPC]Central Nervous System Stimulation [PE]

Selected Package

62037-0734-01Selected

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62037-734-01)