NDC 72162-1284 – Dexmethylphenidate Hydrochloride

Dexmethylphenidate Hydrochloride 2.5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC72162-1284

Product details

Brand name
Dexmethylphenidate Hydrochloride
Generic name
Dexmethylphenidate hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207901
Marketed since
November 30, 2001
Listing expires
December 31, 2026
Pharmacologic class
Central Nervous System Stimulant

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
72162-1284-1100 TABLET in 1 BOTTLE, PLASTIC (72162-1284-1)Feb 1, 2024

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