NDC 0093-5562 – Dexmethylphenidate Hydrochloride

Dexmethylphenidate Hydrochloride 40 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC0093-5562

Product details

Brand name
Dexmethylphenidate Hydrochloride
Generic name
Dexmethylphenidate Hydrochloride
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA202731
Marketed since
November 21, 2013
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
0093-5562-01100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5562-01)Nov 21, 2013

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