Nifurtimox 30 MG Oral Tablet — RxCUI 2395842
RxNorm drug concept · Semantic clinical drug
RxCUI 2395842
Semantic clinical drug · SCD
● Current RxNorm concept 2 FDA products
2 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
RxCUI2395842
Official nameNifurtimox 30 MG Oral Tablet
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
FDA products mapped2
Package NDCs mapped2
RxNorm release07/06/2026
Snapshot dataJul 14, 2026
📖 Skip the Codes — Read It in Plain English.
Our pharmacist-built guide to Nifurtimox: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
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- Yes, every dose — all three times a day — must be taken with food. This isn't just a suggestion. Taking Lampit with food significantly increases the amount of medicine your child a...
- Does my child have to take this with food every single time?
🕸️ Concept Web — How Nifurtimox 30 MG Oral Tablet 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
Nifurtimox 30 MG Oral Tablet
RxCUI 2395842 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.
-
Nifurtimox
7421IN
-
Nifurtimox
-
Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
-
Lampit
2397986BN
-
Lampit
-
Dose forms 9
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
-
Nifurtimox Oral Tablet
446700SCDF -
Nifurtimox Oral Product
1159226SCDG -
Nifurtimox Pill
1159227SCDG -
Nifurtimox Oral Tablet [Lampit]
2397988SBDF -
Lampit Oral Product
2397989SBDG -
Lampit Pill
2397990SBDG -
Oral Tablet
317541DF -
Oral Product
1151131DFG - +1 more in this family
-
Nifurtimox Oral Tablet
-
Clinical & branded drugs 3
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
-
Nifurtimox 30 MG
2395841SCDC -
Nifurtimox 30 MG Oral Tablet [Lampit]
2397991SBD -
Nifurtimox 30 MG [Lampit]
2397987SBDC
-
Nifurtimox 30 MG
Showing up to 8 concepts per family — 13 of 14 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
-
Nifurtimox 30 MG
SCDC · 2395841 -
Nifurtimox Oral Tablet
SCDF · 446700 -
Nifurtimox Oral Product
SCDG · 1159226 -
Nifurtimox Pill
SCDG · 1159227
Brand-Name Concepts
-
Nifurtimox 30 MG Oral Tablet [Lampit]
SBD · 2397991 -
Nifurtimox 30 MG [Lampit]
SBDC · 2397987 -
Nifurtimox Oral Tablet [Lampit]
SBDF · 2397988 -
Lampit Oral Product
SBDG · 2397989 -
Lampit Pill
SBDG · 2397990 -
Lampit
BN · 2397986
📦 FDA Products & Package NDCs
2 products · 2 package NDCs
2 package NDCs map to RxCUI 2395842 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 |
|---|---|---|---|---|
| 50419-0750-01 | 1 BOTTLE in 1 CARTON (50419-750-01) / 100 TABLET, FILM COAT... | LAMPIT | Bayer HealthCare Pharmaceuticals Inc. | 2020-10-01 |
| 50419-0751-01 | 1 BOTTLE in 1 CARTON (50419-751-01) / 100 TABLET, FILM COAT... | LAMPIT | Bayer HealthCare Pharmaceuticals Inc. | 2020-10-01 |
Observed labelers:
Bayer HealthCare Pharmaceuticals Inc. (2)
— 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.