# Trientine hydrochloride

NDC: 72205-008
Generic name: Trientine hydrochloride
Labeler / Manufacturer: Novadoz Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20190522

FDA application: ANDA211134

## Active ingredients

- TRIENTINE HYDROCHLORIDE: 250 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72205-008"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72205-008
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6bc468ca-07ef-4965-b502-0330b76455a0