trientine hydrochloride
Generic: trientine hydrochloride
Labeler: navinta llcDrug Facts
Product Profile
Brand Name
trientine hydrochloride
Generic Name
trientine hydrochloride
Labeler
navinta llc
Dosage Form
CAPSULE
Routes
Active Ingredients
trientine hydrochloride 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68475-200
Product ID
68475-200_57f9ea43-344a-4050-ab62-4087d5961767
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211251
Listing Expiration
2026-12-31
Marketing Start
2020-12-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68475200
Hyphenated Format
68475-200
Supplemental Identifiers
RxCUI
UPC
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
ANDA211251 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (68475-200-01) / 100 CAPSULE in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "57f9ea43-344a-4050-ab62-4087d5961767", "openfda": {"upc": ["0368475200012"], "unii": ["HC3NX54582"], "rxcui": ["313472"], "spl_set_id": ["4c9233bd-be3d-46f0-8fa9-a17e61b1b9a8"], "manufacturer_name": ["Navinta LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68475-200-01) / 100 CAPSULE in 1 BOTTLE", "package_ndc": "68475-200-01", "marketing_start_date": "20201205"}], "brand_name": "Trientine Hydrochloride", "product_id": "68475-200_57f9ea43-344a-4050-ab62-4087d5961767", "dosage_form": "CAPSULE", "pharm_class": ["Copper Chelating Activity [MoA]", "Copper Chelator [EPC]", "Metal Chelating Activity [MoA]"], "product_ndc": "68475-200", "generic_name": "Trientine Hydrochloride", "labeler_name": "Navinta LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trientine Hydrochloride", "active_ingredients": [{"name": "TRIENTINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA211251", "marketing_category": "ANDA", "marketing_start_date": "20201205", "listing_expiration_date": "20261231"}