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: 0591-3869_1895894a-ed70-4f82-b512-6bc184ee806c
Product NDC: 0591-3869
Form: CAPSULE, EXTENDED RELEASE
Composition / generic term: methylphenidate hydrochloride
Labeler: Actavis Pharma, Inc.
Marketing category: ANDA
Marketing start / end (source format): 20200930
Source listing expiry: 20261231

Source-listed ingredients

METHYLPHENIDATE HYDROCHLORIDE — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0591-3869-19) · 0591-3869-19

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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