NDC 72162-2086 – Methylphenidate Hydrochloride

Methylphenidate Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC72162-2086

Product details

Brand name
Methylphenidate Hydrochloride
Generic name
Methylphenidate Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA091159
Marketed since
April 7, 2014
Listing expires
December 31, 2026
Pharmacologic class
Central Nervous System Stimulant

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
72162-2086-1100 TABLET in 1 BOTTLE (72162-2086-1)Apr 3, 2024

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