NDC 49884-339 – Dexmethylphenidate Hydrochloride

Dexmethylphenidate Hydrochloride 35 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC49884-339

Product details

Brand name
Dexmethylphenidate Hydrochloride
Generic name
Dexmethylphenidate Hydrochloride
Labeler
Par Health USA, LLC
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA202842
Marketed since
January 5, 2017
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
49884-339-01100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (49884-339-01)Jan 5, 2017

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