FDA NDC Directory · JSON-LD · Markdown

TRIENTINE HYDROCHLORIDE

NDC 31722-683 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerCamber Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA216356
Dosage form / routeCAPSULE · ORAL
Active ingredientsTRIENTINE HYDROCHLORIDE (250 mg/1)
Marketing started20220623
Package count1

External sources

Source: openFDA. Public-domain (CC0).