FDA NDC Directory · JSON-LD · Markdown

Trientine Hydrochloride

NDC 16571-812 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA212238
Dosage form / routeCAPSULE · ORAL
Active ingredientsTRIENTINE HYDROCHLORIDE (500 mg/1)
Marketing started20230922
Package count1

External sources

Source: openFDA. Public-domain (CC0).