FDA NDC Directory · JSON-LD · Markdown

Trientine Hydrochloride

NDC 68475-200 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerNavinta LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA211251
Dosage form / routeCAPSULE · ORAL
Active ingredientsTRIENTINE HYDROCHLORIDE (250 mg/1)
Marketing started20201205
Package count1

External sources

Source: openFDA. Public-domain (CC0).