NDC 13811-700 – Methylphenidate Hydrochloride

Methylphenidate Hydrochloride 63 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC13811-700

Product details

Brand name
Methylphenidate Hydrochloride
Generic name
Methylphenidate hydrochloride
Labeler
Trigen Laboratories, LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA216117
Marketed since
June 23, 2022
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
13811-700-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-700-30)Jun 23, 2022

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