NDC 0781-2384 – Methylphenidate

Methylphenidate Hydrochloride 20 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC0781-2384

Product details

Brand name
Methylphenidate
Generic name
Methylphenidate
Labeler
Sandoz Inc
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA021284
Marketed since
November 24, 2015
Listing expires
December 31, 2026
Pharmacologic class
Central Nervous System Stimulant

Active ingredients

Uses, dosage, side effects and warnings for Methylphenidate →

Package NDC codes (1)

Package NDCDescriptionSince
0781-2384-01100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0781-2384-01)Feb 20, 2025

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