Package 72205-008-91

Brand: trientine hydrochloride

Generic: trientine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72205-008-91
Digits Only 7220500891
Product NDC 72205-008
Description

1 BOTTLE in 1 CARTON (72205-008-91) / 100 CAPSULE in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2019-05-22
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": "da623cb5-cd76-4236-87ad-212e25349fcd", "openfda": {"upc": ["0372205008915"], "unii": ["HC3NX54582"], "rxcui": ["313472"], "spl_set_id": ["6bc468ca-07ef-4965-b502-0330b76455a0"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (72205-008-91)  / 100 CAPSULE in 1 BOTTLE", "package_ndc": "72205-008-91", "marketing_start_date": "20190522"}], "brand_name": "Trientine hydrochloride", "product_id": "72205-008_da623cb5-cd76-4236-87ad-212e25349fcd", "dosage_form": "CAPSULE", "pharm_class": ["Metal Chelating Activity [MoA]", "Metal Chelator [EPC]"], "product_ndc": "72205-008", "generic_name": "Trientine hydrochloride", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trientine hydrochloride", "active_ingredients": [{"name": "TRIENTINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA211134", "marketing_category": "ANDA", "marketing_start_date": "20190522", "listing_expiration_date": "20261231"}