trientine hydrochloride

Generic: trientine hydrochloride

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

Drug Facts

Product Profile

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

trientine hydrochloride 500 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 16571-812
Product ID 16571-812_96619f61-e1f2-4ed3-9a81-c05077c8cbcb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212238
Listing Expiration 2026-12-31
Marketing Start 2023-09-22

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 16571812
Hyphenated Format 16571-812

Supplemental Identifiers

RxCUI
313472 2619912
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 ANDA212238 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 50 CAPSULE in 1 BOTTLE (16571-812-05)
source: ndc

Packages (1)

16571-812-05 50 CAPSULE in 1 BOTTLE (16571-812-05)

Ingredients (1)

trientine hydrochloride (500 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": "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": "50 CAPSULE in 1 BOTTLE (16571-812-05)", "package_ndc": "16571-812-05", "marketing_start_date": "20230922"}], "brand_name": "Trientine Hydrochloride", "product_id": "16571-812_96619f61-e1f2-4ed3-9a81-c05077c8cbcb", "dosage_form": "CAPSULE", "pharm_class": ["Copper Chelating Activity [MoA]", "Copper Chelator [EPC]", "Metal Chelating Activity [MoA]"], "product_ndc": "16571-812", "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": "500 mg/1"}], "application_number": "ANDA212238", "marketing_category": "ANDA", "marketing_start_date": "20230922", "listing_expiration_date": "20261231"}