trientine hydrochloride
Generic: trientine hydrochloride
Labeler: dr.reddys laboratories incDrug Facts
Product Profile
Brand Name
trientine hydrochloride
Generic Name
trientine hydrochloride
Labeler
dr.reddys laboratories inc
Dosage Form
CAPSULE
Routes
Active Ingredients
trientine hydrochloride 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43598-459
Product ID
43598-459_bdfcecdc-5523-2091-0405-62d51c91e287
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211076
Listing Expiration
2026-12-31
Marketing Start
2019-07-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43598459
Hyphenated Format
43598-459
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ANDA211076 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (43598-459-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
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"}