NDC 0591-3862 – Methylphenidate hydrochloride

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

Human Prescription Drug DEA schedule CII

Product NDC0591-3862

Product details

Brand name
Methylphenidate hydrochloride
Generic name
Methylphenidate hydrochloride
Labeler
Actavis Pharma, Inc.
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA208861
Marketed since
September 30, 2020
Listing expires
December 31, 2026
Pharmacologic class
Central Nervous System Stimulant

Active ingredients

Uses, dosage, side effects and warnings for Methylphenidate Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
0591-3862-1990 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0591-3862-19)Sep 30, 2020

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