United States · FDA National Drug Code directory

Trientine 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
49884-060_c630e57d-26e9-4670-9d3d-fa574857f752
Product NDC
49884-060
Form
CAPSULE
Composition / generic term
Trientine Hydrochloride
Labeler
Par Health USA, LLC
Marketing category
ANDA
Marketing start / end (source format)
20190927 / 20270531

Source-listed ingredients

  • TRIENTINE HYDROCHLORIDE — 250 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 CAPSULE in 1 BOTTLE (49884-060-01) · 49884-060-01

Source and coverage

Open FDA National Drug Code directory

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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