Package 0591-4910-01

Brand: trientine hydrochloride

Generic: trientine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0591-4910-01
Digits Only 0591491001
Product NDC 0591-4910
Description

100 CAPSULE in 1 BOTTLE (0591-4910-01)

Marketing

Marketing Status
Discontinued 2026-04-30
Brand trientine hydrochloride
Generic trientine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fbcd067c-9642-44a1-8f4f-99b49a2e2e7a", "openfda": {"unii": ["HC3NX54582"], "rxcui": ["313472"], "spl_set_id": ["89970c97-2535-4856-b155-62d195b5147c"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0591-4910-01)", "package_ndc": "0591-4910-01", "marketing_end_date": "20260430", "marketing_start_date": "20180208"}], "brand_name": "Trientine Hydrochloride", "product_id": "0591-4910_fbcd067c-9642-44a1-8f4f-99b49a2e2e7a", "dosage_form": "CAPSULE", "pharm_class": ["Copper Chelating Activity [MoA]", "Copper Chelator [EPC]", "Metal Chelating Activity [MoA]"], "product_ndc": "0591-4910", "generic_name": "Trientine Hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trientine Hydrochloride", "active_ingredients": [{"name": "TRIENTINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA207567", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20180208"}