NDC 0115-1741 – Methylphenidate Hydrochloride

Methylphenidate Hydrochloride 60 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC0115-1741

Product details

Brand name
Methylphenidate Hydrochloride
Generic name
Methylphenidate Hydrochloride
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA205105
Marketed since
September 20, 2016
Listing expires
December 31, 2027
Pharmacologic class
Central Nervous System Stimulant

Active ingredients

Uses, dosage, side effects and warnings for Methylphenidate Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
0115-1741-01100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0115-1741-01)Sep 20, 2016

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