Package 68475-200-01

Brand: trientine hydrochloride

Generic: trientine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68475-200-01
Digits Only 6847520001
Product NDC 68475-200
Description

1 BOTTLE in 1 CARTON (68475-200-01) / 100 CAPSULE in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2020-12-05
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": "57f9ea43-344a-4050-ab62-4087d5961767", "openfda": {"upc": ["0368475200012"], "unii": ["HC3NX54582"], "rxcui": ["313472"], "spl_set_id": ["4c9233bd-be3d-46f0-8fa9-a17e61b1b9a8"], "manufacturer_name": ["Navinta LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68475-200-01)  / 100 CAPSULE in 1 BOTTLE", "package_ndc": "68475-200-01", "marketing_start_date": "20201205"}], "brand_name": "Trientine Hydrochloride", "product_id": "68475-200_57f9ea43-344a-4050-ab62-4087d5961767", "dosage_form": "CAPSULE", "pharm_class": ["Copper Chelating Activity [MoA]", "Copper Chelator [EPC]", "Metal Chelating Activity [MoA]"], "product_ndc": "68475-200", "generic_name": "Trientine Hydrochloride", "labeler_name": "Navinta LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trientine Hydrochloride", "active_ingredients": [{"name": "TRIENTINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA211251", "marketing_category": "ANDA", "marketing_start_date": "20201205", "listing_expiration_date": "20261231"}