NDC 0115-9920 – Dexmethylphenidate hydrochloride

Dexmethylphenidate Hydrochloride 15 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC0115-9920

Product details

Brand name
Dexmethylphenidate hydrochloride
Generic name
Dexmethylphenidate hydrochloride
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA079108
Marketed since
November 11, 2014
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 (1)

Package NDCDescriptionSince
0115-9920-01100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0115-9920-01)Nov 11, 2014

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