United States · FDA National Drug Code directory

Methylphenidate Hydrochloride

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
13811-700_ba649db4-df0d-4587-8370-3f866e66e54b
Product NDC
13811-700
Form
TABLET, EXTENDED RELEASE
Composition / generic term
Methylphenidate hydrochloride
Labeler
Trigen Laboratories, LLC
Marketing category
NDA AUTHORIZED GENERIC
Marketing start / end (source format)
20220623
Source listing expiry
20261231

Source-listed ingredients

  • METHYLPHENIDATE HYDROCHLORIDE — 63 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-700-30) · 13811-700-30

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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