# Trientine Hydrochloride

NDC: 68475-200
Generic name: Trientine Hydrochloride
Labeler / Manufacturer: Navinta LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20201205

FDA application: ANDA211251

## Active ingredients

- TRIENTINE HYDROCHLORIDE: 250 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68475-200"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68475-200
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4c9233bd-be3d-46f0-8fa9-a17e61b1b9a8