5 ML cerliponase alfa 30 MG/ML Injection — RxCUI 1922453
RxNorm drug concept · Semantic clinical drug
RxCUI 1922453
Semantic clinical drug · SCD
● 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
RxCUI1922453
Official name5 ML cerliponase alfa 30 MG/ML Injection
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known ascerliponase alfa 150 MG per 5 ML Intraventricular Injection; cerliponase alfa 150 MG in 5 mL Intraventricular Injection
FDA products mapped1
Package NDCs mapped1
Reported Medicaid activity (SDUD)105 prescriptions · 2 state & territory Medicaid programs · latest period Q4 2025
RxNorm release07/06/2026
Snapshot dataJul 14, 2026
🕸️ Concept Web — How 5 ML cerliponase alfa 30 MG/ML Injection 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
5 ML cerliponase alfa 30 MG/ML Injection
RxCUI 1922453 Semantic clinical drug · SCD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
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Ingredients 2
The active substance itself — no strength, form, or brand attached yet.
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Cerliponase
1922437IN -
Cerliponase alfa
1922436PIN
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Cerliponase
-
Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
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Brineura
1922454BN
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Brineura
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Dose forms 9
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
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Cerliponase Injection
1922452SCDF -
Cerliponase alfa Injection
2647003SCDFP -
Cerliponase Injectable Product
1922451SCDG -
Cerliponase alfa Injectable Product
2660087SCDGP -
Cerliponase Injection [Brineura]
1922456SBDF -
Cerliponase alfa Injection [Brineura]
2654385SBDFP -
Brineura Injectable Product
1922457SBDG -
Injection
1649574DF - +1 more in this family
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Cerliponase Injection
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Clinical & branded drugs 3
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
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Cerliponase alfa 30 MG/ML
1922450SCDC -
5 ML cerliponase alfa 30 MG/ML Injection [Brineura]
1922458SBD -
Cerliponase alfa 30 MG/ML [Brineura]
1922455SBDC
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Cerliponase alfa 30 MG/ML
Showing up to 8 concepts per family — 14 of 15 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
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Cerliponase alfa 30 MG/ML
SCDC · 1922450 -
Cerliponase Injection
SCDF · 1922452 -
Cerliponase alfa Injection
SCDFP · 2647003 -
Cerliponase Injectable Product
SCDG · 1922451 -
Cerliponase alfa Injectable Product
SCDGP · 2660087
Brand-Name Concepts
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5 ML cerliponase alfa 30 MG/ML Injection [Brineura]
SBD · 1922458 -
Cerliponase alfa 30 MG/ML [Brineura]
SBDC · 1922455 -
Cerliponase Injection [Brineura]
SBDF · 1922456 -
Cerliponase alfa Injection [Brineura]
SBDFP · 2654385 -
Brineura Injectable Product
SBDG · 1922457 -
Brineura
BN · 1922454
📦 FDA Products & Package NDCs
1 product · 1 package NDC
1 package NDC map to RxCUI 1922453 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 |
|---|---|---|---|---|
| 68135-0811-02 | 1 KIT in 1 CARTON (68135-811-02) * 5 mL in 1 VIAL, GLASS (... | Brineura | BioMarin Pharmaceutical Inc. | 2017-04-27 |
Observed labelers:
BioMarin Pharmaceutical Inc. (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.
Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.