United States · FDA National Drug Code directory

Dexmethylphenidate Hydrochloride Extended-Release

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
49884-430_47a67542-0c06-4542-e063-6394a90a8bfe
Product NDC
49884-430
Form
CAPSULE, EXTENDED RELEASE
Composition / generic term
Dexmethylphenidate Hydrochloride
Labeler
Par Health USA, LLC
Marketing category
ANDA
Marketing start / end (source format)
20131119
Source listing expiry
20271231

Source-listed ingredients

  • DEXMETHYLPHENIDATE HYDROCHLORIDE — 30 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (49884-430-01) · 49884-430-01
  • 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (49884-430-10) · 49884-430-10

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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