NDCFind

Methylphenidate Hydrochloride 57664-0609-88

Package NDC

57664-0609-88

Product NDC: 57664-0609

Manufacturer
Sun Pharmaceutical Industries, Inc.
Dosage Form
Tablet, Extended Release
Route
Oral
Product Type
Human Prescription Drug
DEA Schedule
Schedule CII
Marketing Start
August 20, 2020
Listing Expires
December 31, 2027
Application
ANDA205135

Active Ingredients

IngredientStrength
Methylphenidate Hydrochloride54 mg/1

Drug Class

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

Selected Package

57664-0609-88Selected

100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (57664-609-88)