Package 43598-459-01

Brand: trientine hydrochloride

Generic: trientine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43598-459-01
Digits Only 4359845901
Product NDC 43598-459
Product ID 43598-459_bdfcecdc-5523-2091-0405-62d51c91e287
Description

100 CAPSULE in 1 BOTTLE (43598-459-01)

Marketing

Marketing Status
Marketed Since 2019-07-03
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": "bdfcecdc-5523-2091-0405-62d51c91e287", "openfda": {"unii": ["HC3NX54582"], "rxcui": ["313472"], "spl_set_id": ["fff41159-af99-94bf-4327-8a6a7ee77b36"], "manufacturer_name": ["Dr.Reddys Laboratories Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (43598-459-01)", "package_ndc": "43598-459-01", "marketing_start_date": "20190703"}], "brand_name": "Trientine Hydrochloride", "product_id": "43598-459_bdfcecdc-5523-2091-0405-62d51c91e287", "dosage_form": "CAPSULE", "pharm_class": ["Copper Chelating Activity [MoA]", "Copper Chelator [EPC]", "Metal Chelating Activity [MoA]"], "product_ndc": "43598-459", "generic_name": "Trientine Hydrochloride", "labeler_name": "Dr.Reddys Laboratories Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trientine Hydrochloride", "active_ingredients": [{"name": "TRIENTINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA211076", "marketing_category": "ANDA", "marketing_start_date": "20190703", "listing_expiration_date": "20261231"}