NDC 72162-2394 – Methylphenidate Hydrochloride

Methylphenidate Hydrochloride 36 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC72162-2394

Product details

Brand name
Methylphenidate Hydrochloride
Generic name
Methylphenidate Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA091695
Marketed since
September 23, 2013
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
72162-2394-1100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2394-1)Mar 17, 2026

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