trientine hydrochloride

Generic: trientine hydrochloride

Labeler: actavis pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trientine hydrochloride
Generic Name trientine hydrochloride
Labeler actavis pharma, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

trientine hydrochloride 250 mg/1

Manufacturer
Actavis Pharma, Inc.

Identifiers & Regulatory

Product NDC 0591-4910
Product ID 0591-4910_fbcd067c-9642-44a1-8f4f-99b49a2e2e7a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207567
Marketing Start 2018-02-08
Marketing End 2026-04-30

Pharmacologic Class

Classes
copper chelating activity [moa] copper chelator [epc] metal chelating activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05914910
Hyphenated Format 0591-4910

Supplemental Identifiers

RxCUI
313472
UNII
HC3NX54582

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name trientine hydrochloride (source: ndc)
Generic Name trientine hydrochloride (source: ndc)
Application Number ANDA207567 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (0591-4910-01)
source: ndc

Packages (1)

0591-4910-01 100 CAPSULE in 1 BOTTLE (0591-4910-01)

Ingredients (1)

trientine hydrochloride (250 mg/1)

Linked Drug Pages (1)

Trientine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fbcd067c-9642-44a1-8f4f-99b49a2e2e7a", "openfda": {"unii": ["HC3NX54582"], "rxcui": ["313472"], "spl_set_id": ["89970c97-2535-4856-b155-62d195b5147c"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0591-4910-01)", "package_ndc": "0591-4910-01", "marketing_end_date": "20260430", "marketing_start_date": "20180208"}], "brand_name": "Trientine Hydrochloride", "product_id": "0591-4910_fbcd067c-9642-44a1-8f4f-99b49a2e2e7a", "dosage_form": "CAPSULE", "pharm_class": ["Copper Chelating Activity [MoA]", "Copper Chelator [EPC]", "Metal Chelating Activity [MoA]"], "product_ndc": "0591-4910", "generic_name": "Trientine Hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trientine Hydrochloride", "active_ingredients": [{"name": "TRIENTINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA207567", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20180208"}