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Trientine hydrochloride 250 MG Oral Capsule [Syprine] — RxCUI 208720

RxNorm drug concept · Semantic branded drug
RxCUI 208720 Semantic branded drug · SBD ● Current RxNorm concept 1 FDA product 1 package NDC Snapshot Jul 14, 2026

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Compiled from public NLM RxNorm and FDA (openFDA NDC directory) data sources. Editorial policy

What you’re looking at: the standardized identity of one medicine, as the U.S. drug-data system sees it. Below — every FDA-listed product, package code, price benchmark, and billing code that maps to it.

🗂️ Key Facts

RxCUI208720
Official nameTrientine hydrochloride 250 MG Oral Capsule [Syprine]
Concept typeSemantic branded drug (SBD)
RxNorm statusCurrent RxNorm concept
Also known asSyprine 250 MG Oral Capsule
FDA products mapped1
Package NDCs mapped1
RxNorm release07/06/2026
Snapshot dataJul 14, 2026

🕸️ Concept Web — How Trientine hydrochloride 250 MG Oral Capsule [Syp... Connects

One RxCUI never lives alone. Follow the path from the raw ingredient down to the exact strength-and-form concepts FDA products carry — every stop is a real RxNorm concept with its own identifier. Hover or focus any chip for what it means.
This page's concept Trientine hydrochloride 250 MG Oral Capsule [Syprine] RxCUI 208720

Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.

  1. Ingredients 2

    The active substance itself — no strength, form, or brand attached yet.

    • Trientine 10798
    • Trientine hydrochloride 235370
  2. Brand names 1

    The same medicine's trade names. A brand name alone says nothing about strength or form.

    • Syprine 220145
  3. Dose forms 13

    The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.

    • Trientine Oral Capsule 374205
    • Trientine hydrochloride Oral Capsule 2648964
    • Trientine Oral Product 1158785
    • Trientine Pill 1158786
    • Trientine hydrochloride Oral Product 2659565
    • Trientine hydrochloride Pill 2660172
    • Trientine Oral Capsule [Syprine] 366697
    • Trientine hydrochloride Oral Capsule [Syprine] 2655833
    • +5 more in this family
  4. Clinical & branded drugs 3

    Ingredient + strength + dose form. These are the concepts real FDA products actually carry.

Showing up to 8 concepts per family — 14 of 19 stored related concepts drawn.
These are official RxNorm vocabulary relationships — how concepts name and organize the same medicine. They do not establish therapeutic equivalence or substitutability: two concepts appearing in one web is never a statement that products can be swapped.

🔀 Generic ⇄ Brand Crosswalk

The same medicine has an unbranded (generic) identity and one or more brand-name identities — each with its own RxCUI. This is a naming relationship in RxNorm, not a statement that any two products are substitutable.

Generic (Clinical) Concepts

  • Trientine hydrochloride 250 MG Oral Capsule SCD · 313472
  • Trientine hydrochloride 250 MG SCDC · 1944626
  • Trientine Oral Capsule SCDF · 374205
  • Trientine hydrochloride Oral Capsule SCDFP · 2648964
  • Trientine Oral Product SCDG · 1158785
  • Trientine Pill SCDG · 1158786
  • Trientine hydrochloride Oral Product SCDGP · 2659565
  • Trientine hydrochloride Pill SCDGP · 2660172

Brand-Name Concepts

  • Trientine hydrochloride 250 MG [Syprine] SBDC · 1944628
  • Trientine Oral Capsule [Syprine] SBDF · 366697
  • Trientine hydrochloride Oral Capsule [Syprine] SBDFP · 2655833
  • Syprine Oral Product SBDG · 1186078
  • Syprine Pill SBDG · 1186079
  • Syprine BN · 220145

📦 FDA Products & Package NDCs

1 product · 1 package NDC
1 package NDC map to RxCUI 208720 in the current snapshot — up to 50 per page. Each linked NDC opens its full package page.
Package NDC Package Brand / generic name Labeler Marketing start
00187-2120-10 1 BOTTLE in 1 CARTON (0187-2120-10) / 100 CAPSULE in 1 BOTT... Syprine Bausch Health US LLC 1985-11-08
Observed labelers: Bausch Health US LLC (1) — this is the FDA-listed mapping footprint, not sales, inventory, availability, or market share.

🗃️ Sources & Limits

Atlas generation902fddb9-e9c1-4004-bf4c-dba4d51037c7
openFDA export observedJul 14, 2026
RxNorm release07/06/2026
Methodology2026-07-full-catalog-v1
  • A shared RxCUI does not prove interchangeability. Products mapped to the same concept are not thereby equivalent or substitutable — equivalence is a separate, product-level determination.
  • Listing here does not establish approval or coverage. Appearing in this snapshot is a data observation, not an FDA approval status or a payer coverage decision.
  • Missing data never means zero. A silent dataset (no price, no billing code, no utilization) means no observation — not that the real-world value is zero.
  • Counts describe the mapping footprint. Product, package, and labeler counts are the FDA-listed mapping footprint in this snapshot — not sales, inventory, availability, or market share.
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.

Machine-readable JSON

Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.