Package 16571-810-01

Brand: trientine hydrochloride

Generic: trientine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 16571-810-01
Digits Only 1657181001
Product NDC 16571-810
Product ID 16571-810_96619f61-e1f2-4ed3-9a81-c05077c8cbcb
Description

100 CAPSULE in 1 BOTTLE (16571-810-01)

Marketing

Marketing Status
Marketed Since 2021-03-30
Brand trientine hydrochloride
Generic trientine hydrochloride
Sample Package No

Linked Drug Pages (1)

Trientine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "96619f61-e1f2-4ed3-9a81-c05077c8cbcb", "openfda": {"unii": ["HC3NX54582"], "rxcui": ["313472", "2619912"], "spl_set_id": ["f33c1322-f7c0-4684-afc8-8caa3f4023dc"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (16571-810-01)", "package_ndc": "16571-810-01", "marketing_start_date": "20210330"}], "brand_name": "Trientine Hydrochloride", "product_id": "16571-810_96619f61-e1f2-4ed3-9a81-c05077c8cbcb", "dosage_form": "CAPSULE", "pharm_class": ["Copper Chelating Activity [MoA]", "Copper Chelator [EPC]", "Metal Chelating Activity [MoA]"], "product_ndc": "16571-810", "generic_name": "Trientine Hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trientine Hydrochloride", "active_ingredients": [{"name": "TRIENTINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA212238", "marketing_category": "ANDA", "marketing_start_date": "20210330", "listing_expiration_date": "20261231"}