Package 49884-060-01

Brand: trientine hydrochloride

Generic: trientine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 49884-060-01
Digits Only 4988406001
Product NDC 49884-060
Description

100 CAPSULE in 1 BOTTLE (49884-060-01)

Marketing

Marketing Status
Marketed Since 2019-09-27
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": "c7a6e9ee-c638-4802-8966-ecd293d4f834", "openfda": {"upc": ["0349884060015"], "unii": ["HC3NX54582"], "rxcui": ["313472"], "spl_set_id": ["431c7f66-d58b-4eb0-b195-d164788f9acf"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (49884-060-01)", "package_ndc": "49884-060-01", "marketing_start_date": "20190927"}], "brand_name": "Trientine Hydrochloride", "product_id": "49884-060_c7a6e9ee-c638-4802-8966-ecd293d4f834", "dosage_form": "CAPSULE", "pharm_class": ["Copper Chelating Activity [MoA]", "Copper Chelator [EPC]", "Metal Chelating Activity [MoA]"], "product_ndc": "49884-060", "generic_name": "Trientine Hydrochloride", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trientine Hydrochloride", "active_ingredients": [{"name": "TRIENTINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA210096", "marketing_category": "ANDA", "marketing_start_date": "20190927", "listing_expiration_date": "20261231"}