NDC 63629-2306 – Dexmethylphenidate Hydrochloride

Dexmethylphenidate Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC63629-2306

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
63629-2306-1100 TABLET in 1 BOTTLE, PLASTIC (63629-2306-1)Dec 22, 2021

Other Dexmethylphenidate Hydrochloride products