NDC 72162-2426 – Dexmethylphenidate hydrochloride

Dexmethylphenidate Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC72162-2426

Product details

Brand name
Dexmethylphenidate hydrochloride
Generic name
Dexmethylphenidate hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209211
Marketed since
May 3, 2024
Listing expires
December 31, 2027
Pharmacologic class
Central Nervous System Stimulant

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
72162-2426-1100 TABLET in 1 BOTTLE (72162-2426-1)Mar 17, 2026
72162-2426-660 TABLET in 1 BOTTLE (72162-2426-6)Mar 17, 2026

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