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Polyethylene glycol 3350 420000 MG / potassium chloride 1480 MG / sodium bicarbonate 5720... — RxCUI 904158

RxNorm drug concept · Semantic branded drug
RxCUI 904158 Semantic branded drug · SBD ● Current RxNorm concept 1 FDA product 1 package NDC 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

RxCUI904158
Official namePolyethylene glycol 3350 420000 MG / potassium chloride 1480 MG / sodium bicarbonate 5720 MG / sodium chloride 11200 MG Powder for Oral Solution [TriLyte]
Concept typeSemantic branded drug (SBD)
RxNorm statusCurrent RxNorm concept
Also known asTriLyte (PEG-3350 420 GM / KCL 1.48 GM / NaHCO3 5.72 GM / NaCL 11.2 GM) Powder for 4 L Oral Solution; TriLyte Powder for Oral Solution; POLYETHYLENE GLYCOL 3350 420000 MG / K+ Chloride 1480 MG / NaHCO3 5720 MG / NaCl 11200 MG Powder for Oral Solution [TriLyte]; POLYETHYLENE GLYCOL 3350 420000 MG / Pot Chloride 1480 MG / NaHCO3 5720 MG / NaCl 11200 MG Powder for Oral Solution [TriLyte]; TriLyte (PEG-3350 420 GM / potassium chloride 1.48 GM / sodium bicarbonate 5.72 GM / sodium chloride 11.2 GM) Powder for 4 L Oral Solution
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 Polyethylene Glycol 3350: what it is, how it’s used, side effects, and interactions.

📗 Our plain-language guide HelloPharmacist
  • You can generally expect a bowel movement within 1 to 3 days after taking it. It's not meant to work in an hour like some other laxatives — it works gradually. If you haven't gone...
  • How long does it take for Polyethylene Glycol 3350 to work?
  • You can stir it into any 4 to 8 ounces of beverage — water, juice, coffee, tea, whatever you like, cold or hot. The key is to stir it well until it's completely dissolved. Don't dr...
  • Can I mix it into any drink, or does it have to be water?
📖 Read our full Polyethylene Glycol 3350 guide →

🕸️ Concept Web — How Polyethylene glycol 3350 420000 MG / potassium c... 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 Polyethylene glycol 3350 420000 MG / potassium chloride 1480 MG / sodium bicarbonate 5720 MG / sodium chloride 11200 MG Powder for Oral Solution [TriLyte] RxCUI 904158

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

  1. Ingredients 5

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

    • Polyethylene glycol 3350 221147
    • Potassium chloride 8591
    • Sodium bicarbonate 36676
    • Sodium chloride 9863
    • Polyethylene glycol 3350 / potassium chloride / sodium bicarbonate / sodium chloride 815308
  2. Brand names 1

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

    • TriLyte 763604
  3. Dose forms 9

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

    • Polyethylene glycol 3350 / potassium chloride / sodium bicarbonate / sodium chloride Powder for Oral Solution 1718982
    • Polyethylene glycol 3350 / potassium chloride / sodium bicarbonate / sodium chloride Oral Powder Product 1718981
    • Polyethylene glycol 3350 / potassium chloride / sodium bicarbonate / sodium chloride Oral Product 1162920
    • Polyethylene glycol 3350 / potassium chloride / sodium bicarbonate / sodium chloride Powder for Oral Solution [TriLyte] 1719708
    • TriLyte Oral Powder Product 1719709
    • TriLyte Oral Product 1180359
    • Powder for Oral Solution 1540455
    • Oral Powder Product 1294711
    • +1 more in this family
  4. Clinical & branded drugs 6

    Ingredient + strength + dose form. These are the concepts real FDA products actually carry.

Showing up to 8 concepts per family — 20 of 21 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

Brand-Name Concepts

  • Polyethylene glycol 3350 420000 MG / potassium chloride 1480 MG / sodium bicarbonate 5720 MG / sodium chloride 11200 MG [TriLyte] SBDC · 1719707
  • Polyethylene glycol 3350 / potassium chloride / sodium bicarbonate / sodium chloride Powder for Oral Solution [TriLyte] SBDF · 1719708
  • TriLyte Oral Powder Product SBDG · 1719709
  • TriLyte Oral Product SBDG · 1180359
  • TriLyte BN · 763604

📦 FDA Products & Package NDCs

1 product · 1 package NDC
1 package NDC map to RxCUI 904158 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
84386-0013-04 4 L in 1 BOTTLE (84386-013-04) TRILYTE Aurobindo Pharma Limited 2026-04-14
Observed labelers: Aurobindo Pharma Limited (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.

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.