United States · FDA National Drug Code directory

Dexmethylphenidate 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: 49884-339_09fcee97-8b48-4a1d-a380-0e01c92e0e9b
Product NDC: 49884-339
Form: CAPSULE, EXTENDED RELEASE
Composition / generic term: Dexmethylphenidate Hydrochloride
Labeler: Par Health USA, LLC
Marketing category: ANDA
Marketing start / end (source format): 20170105
Source listing expiry: 20261231

Source-listed ingredients

DEXMETHYLPHENIDATE HYDROCHLORIDE — 35 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (49884-339-01) · 49884-339-01

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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