0.5 ML vutrisiran 50 MG/ML Prefilled Syringe [Amvuttra] — RxCUI 2604794
RxNorm drug concept · Semantic branded drug
RxCUI 2604794
Semantic branded drug · SBD
● Current RxNorm concept 1 FDA product
1 package NDC
Snapshot Jul 14, 2026
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
RxCUI2604794
Official name0.5 ML vutrisiran 50 MG/ML Prefilled Syringe [Amvuttra]
Concept typeSemantic branded drug (SBD)
RxNorm statusCurrent RxNorm concept
Also known as0.5 ML Amvuttra 50 MG/ML Prefilled Syringe; amvuttra 25 MG in 0.5 ML Prefilled Syringe; Amvuttra 25 MG per 0.5 ML Prefilled Syringe
FDA products mapped1
Package NDCs mapped1
RxNorm release07/06/2026
Snapshot dataJul 14, 2026
📖 Skip the Codes — Read It in Plain English.
Our pharmacist-built guide to Vutrisiran Injection: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
- Amvuttra is not a cure, but it's a powerful treatment. You have a condition called transthyretin-mediated amyloidosis, where a protein called TTR misfolds and builds up in your bod...
- What exactly is Amvuttra treating — is it a cure?
- Just once every 3 months — that's only four times a year. It's a subcutaneous injection given by a healthcare professional, similar to a flu shot but under the skin rather than int...
- How often do I need to come in for my injection?
🕸️ Concept Web — How 0.5 ML vutrisiran 50 MG/ML Prefilled Syringe [Am... 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
0.5 ML vutrisiran 50 MG/ML Prefilled Syringe [Amvuttra]
RxCUI 2604794 Semantic branded drug · SBD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
-
Ingredients 1
The active substance itself — no strength, form, or brand attached yet.
-
Vutrisiran
2604578IN
-
Vutrisiran
-
Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
-
Amvuttra
2604790BN
-
Amvuttra
-
Dose forms 6
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
-
Vutrisiran Prefilled Syringe
2604787SCDF -
Vutrisiran Injectable Product
2604786SCDG -
Vutrisiran Prefilled Syringe [Amvuttra]
2604793SBDF -
Amvuttra Injectable Product
2604792SBDG -
Prefilled Syringe
721656DF -
Injectable Product
1151126DFG
-
Vutrisiran Prefilled Syringe
-
Clinical & branded drugs 3
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
-
0.5 ML vutrisiran 50 MG/ML Prefilled Syringe
2604788SCD -
Vutrisiran 50 MG/ML
2604785SCDC -
Vutrisiran 50 MG/ML [Amvuttra]
2604791SBDC
-
0.5 ML vutrisiran 50 MG/ML Prefilled Syringe
Showing up to 8 concepts per family — 11 of 11 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
-
0.5 ML vutrisiran 50 MG/ML Prefilled Syringe
SCD · 2604788 -
Vutrisiran 50 MG/ML
SCDC · 2604785 -
Vutrisiran Prefilled Syringe
SCDF · 2604787 -
Vutrisiran Injectable Product
SCDG · 2604786
Brand-Name Concepts
-
Vutrisiran 50 MG/ML [Amvuttra]
SBDC · 2604791 -
Vutrisiran Prefilled Syringe [Amvuttra]
SBDF · 2604793 -
Amvuttra Injectable Product
SBDG · 2604792 -
Amvuttra
BN · 2604790
📦 FDA Products & Package NDCs
1 product · 1 package NDC
1 package NDC map to RxCUI 2604794 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 |
|---|---|---|---|---|
| 71336-1003-01 | 1 SYRINGE, GLASS in 1 CARTON (71336-1003-1) / .5 mL in 1 SY... | AMVUTTRA | Alnylam Pharmaceuticals, Inc. | 2022-06-13 |
Observed labelers:
Alnylam Pharmaceuticals, Inc. (1)
— this is the FDA-listed mapping footprint, not sales, inventory, availability, or market share.
🧾 Billing Codes (HCPCS)
Medical billing codes (HCPCS "J-codes") that connect to this concept's packages — used mostly when a clinic or hospital bills for a drug it administers. Each code links to its full billing page.
| Code | Descriptor | Mapped packages | Sources |
|---|---|---|---|
| J0225 | Inj, vutrisiran, 1 mg | 1 | CMS |
⚠ A crosswalk is not coverage: an NDC↔HCPCS mapping does not guarantee any payer covers or pays the code. Always verify the current payer policy before billing.
🗃️ 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.
Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.