NDC 0527-8111 – Dexmethylphenidate Hydrochloride Extended-Release

Dexmethylphenidate Hydrochloride 30 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC0527-8111

Product details

Brand name
Dexmethylphenidate Hydrochloride Extended-Release
Generic name
dexmethylphenidate hydrochloride
Labeler
Lannett Company, Inc.
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA210279
Marketed since
October 9, 2018
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
0527-8111-37100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-8111-37)Oct 9, 2018

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