trientine hydrochloride
Generic: trientine hydrochloride
Labeler: endo usa, inc.Drug Facts
Product Profile
Brand Name
trientine hydrochloride
Generic Name
trientine hydrochloride
Labeler
endo usa, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
trientine hydrochloride 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
49884-060
Product ID
49884-060_c7a6e9ee-c638-4802-8966-ecd293d4f834
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210096
Listing Expiration
2026-12-31
Marketing Start
2019-09-27
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
49884060
Hyphenated Format
49884-060
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
ANDA210096 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (49884-060-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c7a6e9ee-c638-4802-8966-ecd293d4f834", "openfda": {"upc": ["0349884060015"], "unii": ["HC3NX54582"], "rxcui": ["313472"], "spl_set_id": ["431c7f66-d58b-4eb0-b195-d164788f9acf"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (49884-060-01)", "package_ndc": "49884-060-01", "marketing_start_date": "20190927"}], "brand_name": "Trientine Hydrochloride", "product_id": "49884-060_c7a6e9ee-c638-4802-8966-ecd293d4f834", "dosage_form": "CAPSULE", "pharm_class": ["Copper Chelating Activity [MoA]", "Copper Chelator [EPC]", "Metal Chelating Activity [MoA]"], "product_ndc": "49884-060", "generic_name": "Trientine Hydrochloride", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trientine Hydrochloride", "active_ingredients": [{"name": "TRIENTINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA210096", "marketing_category": "ANDA", "marketing_start_date": "20190927", "listing_expiration_date": "20261231"}