trientine hydrochloride
Generic: trientine hydrochloride
Labeler: novadoz pharmaceuticals llcDrug Facts
Product Profile
Brand Name
trientine hydrochloride
Generic Name
trientine hydrochloride
Labeler
novadoz pharmaceuticals llc
Dosage Form
CAPSULE
Routes
Active Ingredients
trientine hydrochloride 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72205-008
Product ID
72205-008_da623cb5-cd76-4236-87ad-212e25349fcd
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211134
Listing Expiration
2026-12-31
Marketing Start
2019-05-22
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72205008
Hyphenated Format
72205-008
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
ANDA211134 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (72205-008-91) / 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": "da623cb5-cd76-4236-87ad-212e25349fcd", "openfda": {"upc": ["0372205008915"], "unii": ["HC3NX54582"], "rxcui": ["313472"], "spl_set_id": ["6bc468ca-07ef-4965-b502-0330b76455a0"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (72205-008-91) / 100 CAPSULE in 1 BOTTLE", "package_ndc": "72205-008-91", "marketing_start_date": "20190522"}], "brand_name": "Trientine hydrochloride", "product_id": "72205-008_da623cb5-cd76-4236-87ad-212e25349fcd", "dosage_form": "CAPSULE", "pharm_class": ["Metal Chelating Activity [MoA]", "Metal Chelator [EPC]"], "product_ndc": "72205-008", "generic_name": "Trientine hydrochloride", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trientine hydrochloride", "active_ingredients": [{"name": "TRIENTINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA211134", "marketing_category": "ANDA", "marketing_start_date": "20190522", "listing_expiration_date": "20261231"}