# Trientine Hydrochloride

NDC: 16571-810
Generic name: Trientine Hydrochloride
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20210330

FDA application: ANDA212238

## 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:"16571-810"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16571-810
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f33c1322-f7c0-4684-afc8-8caa3f4023dc