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Felbamate 600 MG Oral Tablet — RxCUI 198359

RxNorm drug concept · Semantic clinical drug
RxCUI 198359 Semantic clinical drug · SCD ● Current RxNorm concept 16 FDA products 46 package NDCs 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

RxCUI198359
Official nameFelbamate 600 MG Oral Tablet
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asFELT 600 MG Oral Tablet
FDA products mapped16
Package NDCs mapped46
Reported Medicaid activity (SDUD)13,974 prescriptions · 39 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 Felbamate: what it is, how it’s used, side effects, and interactions.

📗 Our plain-language guide HelloPharmacist
  • It treats severe epilepsy when other medicines haven't worked well enough. It's used for partial seizures in adults and for Lennox-Gastaut syndrome in children. It isn't a first-ch...
  • You take it by mouth, as tablets or liquid, several times a day. Follow your prescriber's schedule exactly. Never stop it suddenly, because seizures could increase.
  • Common ones include poor appetite, nausea, vomiting, trouble sleeping, headache, dizziness and sleepiness. Tell your doctor if they bother you or don't go away.
  • Call for signs of infection, unusual bleeding or bruising, or unusual paleness. Also call for yellow skin or eyes, dark urine, a serious rash, or any mood changes or thoughts of se...
📖 Read our full Felbamate guide →

🕸️ Concept Web — How Felbamate 600 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 Felbamate 600 MG Oral Tablet RxCUI 198359

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

  1. Ingredients 1

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

    • Felbamate 24812
  2. Brand names 1

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

    • Felbatol 224900
  3. Dose forms 9

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

    • Felbamate Oral Tablet 372145
    • Felbamate Oral Product 1163810
    • Felbamate Pill 1163811
    • Felbamate Oral Tablet [Felbatol] 369165
    • Felbatol Oral Product 1176002
    • Felbatol Pill 1176003
    • Oral Tablet 317541
    • Oral Product 1151131
    • +1 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 — 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

  • Felbamate 600 MG SCDC · 315924
  • Felbamate Oral Tablet SCDF · 372145
  • Felbamate Oral Product SCDG · 1163810
  • Felbamate Pill SCDG · 1163811

Brand-Name Concepts

  • Felbamate 600 MG Oral Tablet [Felbatol] SBD · 209027
  • Felbamate 600 MG [Felbatol] SBDC · 569662
  • Felbamate Oral Tablet [Felbatol] SBDF · 369165
  • Felbatol Oral Product SBDG · 1176002
  • Felbatol Pill SBDG · 1176003
  • Felbatol BN · 224900

📦 FDA Products & Package NDCs

16 products · 46 package NDCs
46 package NDCs map to RxCUI 198359 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
00037-0430-01 100 TABLET in 1 BOTTLE, PLASTIC (0037-0430-01) Felbatol Viatris Specialty LLC 1993-07-29
00037-0431-01 100 TABLET in 1 BOTTLE, PLASTIC (0037-0431-01) Felbatol Viatris Specialty LLC 1993-07-29
51672-4185-01 100 TABLET in 1 BOTTLE (51672-4185-1) Felbamate Sun Pharmaceutical Industries, Inc. 2017-04-20
51672-4185-06 30 TABLET in 1 BOTTLE (51672-4185-6) Felbamate Sun Pharmaceutical Industries, Inc. 2017-04-20
51672-4186-01 100 TABLET in 1 BOTTLE (51672-4186-1) Felbamate Sun Pharmaceutical Industries, Inc. 2017-04-20
51672-4186-06 30 TABLET in 1 BOTTLE (51672-4186-6) Felbamate Sun Pharmaceutical Industries, Inc. 2017-04-20
53746-0734-30 30 TABLET in 1 BOTTLE (53746-734-30) Felbamate Amneal Pharmaceuticals of New York LLC 2022-08-10
53746-0734-90 90 TABLET in 1 BOTTLE (53746-734-90) Felbamate Amneal Pharmaceuticals of New York LLC 2022-08-10
53746-0735-18 180 TABLET in 1 BOTTLE (53746-735-18) Felbamate Amneal Pharmaceuticals of New York LLC 2022-08-10
53746-0735-30 30 TABLET in 1 BOTTLE (53746-735-30) Felbamate Amneal Pharmaceuticals of New York LLC 2022-08-10
53746-0735-90 90 TABLET in 1 BOTTLE (53746-735-90) Felbamate Amneal Pharmaceuticals of New York LLC 2022-08-10
62559-0730-01 100 TABLET in 1 BOTTLE (62559-730-01) Felbamate ANI Pharmaceuticals, Inc. 2018-09-04
62559-0731-01 100 TABLET in 1 BOTTLE (62559-731-01) Felbamate ANI Pharmaceuticals, Inc. 2018-09-04
63629-1944-01 100 TABLET in 1 BOTTLE (63629-1944-1) Felbamate Bryant Ranch Prepack 2021-01-19
65162-0734-03 30 TABLET in 1 BOTTLE (65162-734-03) Felbamate Amneal Pharmaceuticals LLC 2011-09-16
65162-0734-09 90 TABLET in 1 BOTTLE (65162-734-09) Felbamate Amneal Pharmaceuticals LLC 2011-09-16
65162-0734-27 270 TABLET in 1 BOTTLE (65162-734-27) Felbamate Amneal Pharmaceuticals LLC 2011-09-16
65162-0734-50 500 TABLET in 1 BOTTLE (65162-734-50) Felbamate Amneal Pharmaceuticals LLC 2011-09-16
65162-0735-03 30 TABLET in 1 BOTTLE (65162-735-03) Felbamate Amneal Pharmaceuticals LLC 2011-09-16
65162-0735-09 90 TABLET in 1 BOTTLE (65162-735-09) Felbamate Amneal Pharmaceuticals LLC 2011-09-16
65162-0735-18 180 TABLET in 1 BOTTLE (65162-735-18) Felbamate Amneal Pharmaceuticals LLC 2011-09-16
65162-0735-27 270 TABLET in 1 BOTTLE (65162-735-27) Felbamate Amneal Pharmaceuticals LLC 2011-09-16
65162-0735-50 500 TABLET in 1 BOTTLE (65162-735-50) Felbamate Amneal Pharmaceuticals LLC 2011-09-16
70771-1077-01 100 TABLET in 1 BOTTLE (70771-1077-1) Felbamate Zydus Lifesciences Limited 2017-08-15
70771-1077-03 30 TABLET in 1 BOTTLE (70771-1077-3) Felbamate Zydus Lifesciences Limited 2017-08-15
70771-1077-04 10 BLISTER PACK in 1 CARTON (70771-1077-4) / 10 TABLET in 1... Felbamate Zydus Lifesciences Limited 2017-08-15
70771-1077-05 500 TABLET in 1 BOTTLE (70771-1077-5) Felbamate Zydus Lifesciences Limited 2017-08-15
70771-1077-09 90 TABLET in 1 BOTTLE (70771-1077-9) Felbamate Zydus Lifesciences Limited 2017-08-15
70771-1078-01 100 TABLET in 1 BOTTLE (70771-1078-1) Felbamate Zydus Lifesciences Limited 2017-08-15
70771-1078-03 30 TABLET in 1 BOTTLE (70771-1078-3) Felbamate Zydus Lifesciences Limited 2017-08-15
70771-1078-04 10 BLISTER PACK in 1 CARTON (70771-1078-4) / 10 TABLET in 1... Felbamate Zydus Lifesciences Limited 2017-08-15
70771-1078-05 500 TABLET in 1 BOTTLE (70771-1078-5) Felbamate Zydus Lifesciences Limited 2017-08-15
70771-1078-08 180 TABLET in 1 BOTTLE (70771-1078-8) Felbamate Zydus Lifesciences Limited 2017-08-15
70771-1078-09 90 TABLET in 1 BOTTLE (70771-1078-9) Felbamate Zydus Lifesciences Limited 2017-08-15
72162-1771-01 100 TABLET in 1 BOTTLE (72162-1771-1) Felbamate Bryant Ranch Prepack 2026-03-25
72578-0056-01 100 TABLET in 1 BOTTLE (72578-056-01) Felbamate Viona Pharmaceuticals Inc 2020-03-03
72578-0056-05 500 TABLET in 1 BOTTLE (72578-056-05) Felbamate Viona Pharmaceuticals Inc 2020-03-03
72578-0056-06 30 TABLET in 1 BOTTLE (72578-056-06) Felbamate Viona Pharmaceuticals Inc 2020-03-03
72578-0056-16 90 TABLET in 1 BOTTLE (72578-056-16) Felbamate Viona Pharmaceuticals Inc 2020-03-03
72578-0056-77 10 BLISTER PACK in 1 CARTON (72578-056-77) / 10 TABLET in 1... Felbamate Viona Pharmaceuticals Inc 2020-03-03
72578-0057-01 100 TABLET in 1 BOTTLE (72578-057-01) Felbamate Viona Pharmaceuticals Inc 2020-03-03
72578-0057-05 500 TABLET in 1 BOTTLE (72578-057-05) Felbamate Viona Pharmaceuticals Inc 2020-03-03
72578-0057-06 30 TABLET in 1 BOTTLE (72578-057-06) Felbamate Viona Pharmaceuticals Inc 2020-03-03
72578-0057-16 90 TABLET in 1 BOTTLE (72578-057-16) Felbamate Viona Pharmaceuticals Inc 2020-03-03
72578-0057-28 180 TABLET in 1 BOTTLE (72578-057-28) Felbamate Viona Pharmaceuticals Inc 2020-03-03
72578-0057-77 10 BLISTER PACK in 1 CARTON (72578-057-77) / 10 TABLET in 1... Felbamate Viona Pharmaceuticals Inc 2020-03-03
Observed labelers: Viona Pharmaceuticals Inc (11) · Zydus Lifesciences Limited (11) · Amneal Pharmaceuticals LLC (9) · Amneal Pharmaceuticals of New York LLC (5) · Sun Pharmaceutical Industries, Inc. (4) · ANI Pharmaceuticals, Inc. (2) · +2 more — 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.