1 ML guselkumab 100 MG/ML Auto-Injector — RxCUI 2118739
RxNorm drug concept · Semantic clinical drug
RxCUI 2118739
Semantic clinical drug · SCD
● Current RxNorm concept 3 FDA products
10 package NDCs
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
RxCUI2118739
Official name1 ML guselkumab 100 MG/ML Auto-Injector
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asguselkumab 100 MG per 1 ML Auto-Injector; guselkumab 100 MG in 1 ML Auto-Injector
FDA products mapped3
Package NDCs mapped10
Reported Medicaid activity (SDUD)32,717 prescriptions · 47 state & territory Medicaid programs · latest period Q4 2025
RxNorm release07/06/2026
Snapshot dataJul 14, 2026
📖 Skip the Codes — Read It in Plain English.
Our pharmacist-built guide to Guselkumab Injection: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
- Tremfya is approved to treat moderate-to-severe plaque psoriasis and active psoriatic arthritis in adults and in children as young as 6 years old (who weigh at least about 88 lbs)....
- What conditions does Tremfya actually treat?
- Not necessarily. For plaque psoriasis and psoriatic arthritis, Tremfya is given as a subcutaneous injection — meaning under the skin — and adults can self-inject at home using the...
- How do I take this medication — do I have to go to a clinic every time?
🕸️ Concept Web — How 1 ML guselkumab 100 MG/ML Auto-Injector 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
1 ML guselkumab 100 MG/ML Auto-Injector
RxCUI 2118739 Semantic clinical drug · SCD
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.
-
Guselkumab
1928588IN
-
Guselkumab
-
Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
-
Tremfya
1928593BN
-
Tremfya
-
Dose forms 6
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
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Guselkumab Auto-Injector
2118738SCDF -
Guselkumab Injectable Product
1928590SCDG -
Guselkumab Auto-Injector [Tremfya]
2118740SBDF -
Tremfya Injectable Product
1928596SBDG -
Auto-Injector
1649570DF -
Injectable Product
1151126DFG
-
Guselkumab Auto-Injector
-
Clinical & branded drugs 3
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
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Guselkumab 100 MG/ML
1928589SCDC -
1 ML guselkumab 100 MG/ML Auto-Injector [Tremfya]
2118741SBD -
Guselkumab 100 MG/ML [Tremfya]
1928594SBDC
-
Guselkumab 100 MG/ML
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
-
Guselkumab 100 MG/ML
SCDC · 1928589 -
Guselkumab Auto-Injector
SCDF · 2118738 -
Guselkumab Injectable Product
SCDG · 1928590
Brand-Name Concepts
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1 ML guselkumab 100 MG/ML Auto-Injector [Tremfya]
SBD · 2118741 -
Guselkumab 100 MG/ML [Tremfya]
SBDC · 1928594 -
Guselkumab Auto-Injector [Tremfya]
SBDF · 2118740 -
Tremfya Injectable Product
SBDG · 1928596 -
Tremfya
BN · 1928593
📦 FDA Products & Package NDCs
3 products · 10 package NDCs
10 package NDCs map to RxCUI 2118739 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 |
|---|---|---|---|---|
| 57894-0640-01 | 1 SYRINGE in 1 CARTON (57894-640-01) / 1 mL in 1 SYRINGE | TREMFYA | Janssen Biotech, Inc. | 2017-07-13 |
| 57894-0640-04 | 1 SYRINGE in 1 CARTON (57894-640-04) / 1 mL in 1 SYRINGE | TREMFYA | Janssen Biotech, Inc. | 2017-07-13 |
| 57894-0640-06 | 1 SYRINGE in 1 CARTON (57894-640-06) / 1 mL in 1 SYRINGE (5... | TREMFYA | Janssen Biotech, Inc. | 2025-03-25 |
| 57894-0640-11 | 1 SYRINGE in 1 CARTON (57894-640-11) / 1 mL in 1 SYRINGE | TREMFYA | Janssen Biotech, Inc. | 2019-01-28 |
| 57894-0640-99 | 1 SYRINGE in 1 CARTON (57894-640-99) / 1 mL in 1 SYRINGE | TREMFYA | Janssen Biotech, Inc. | 2019-01-28 |
| 57894-0650-02 | 1 VIAL, SINGLE-DOSE in 1 CARTON (57894-650-02) / 20 mL in 1... | TREMFYA | Janssen Biotech, Inc. | 2024-09-11 |
| 57894-0651-02 | 1 SYRINGE in 1 CARTON (57894-651-02) / 2 mL in 1 SYRINGE (5... | TREMFYA | Janssen Biotech, Inc. | 2024-09-11 |
| 57894-0651-04 | 2 CARTON in 1 CARTON (57894-651-04) / 1 SYRINGE in 1 CARTON... | TREMFYA | Janssen Biotech, Inc. | 2025-03-20 |
| 57894-0651-22 | 1 SYRINGE in 1 CARTON (57894-651-22) / 2 mL in 1 SYRINGE (5... | TREMFYA | Janssen Biotech, Inc. | 2024-09-11 |
| 57894-0651-92 | 1 SYRINGE in 1 CARTON (57894-651-92) / 2 mL in 1 SYRINGE (5... | TREMFYA | Janssen Biotech, Inc. | 2024-09-11 |
Observed labelers:
Janssen Biotech, Inc. (10)
— 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 |
|---|---|---|---|
| J1628 | Inj., guselkumab, 1 mg | 7 | 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.