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NITROUS OXIDE 99 L/100L Gas, 3700 l — NDC 42602-0003-09 package photo

NITROUS OXIDE 99 L/100L Gas, 3700 l

by Norco, Inc · 3700 L in 1 CYLINDER (42602-003-09)
NDC 42602-0003-09
🏷️ FDA NDC (as labeled) 42602-003-09 billing pads the product segment with a zero
This package
Contains3700 l Pack sizes9 compare ↓
Rx only Brand On market Non-controlled
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

🆔 Identity & classification

FDA NDC (as labeled) 42602-003-09
Product NDC 42602-003
11-digit billing NDC 42602000309
RxCUI 312022
UNII K50XQU1029
Application # NDA206009
SPL Set ID a5403bef-c22d-4246-be7a-a198aa254001
DEA schedule Non-controlled
Marketing category NDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2008-09-01
Route RESPIRATORY (INHALATION)
Dosage form GAS
Substance NITROUS OXIDE
Why two NDCs? The FDA registers this code as 42602-003-09 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 42602-0003-09. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

🏷️ RxNorm drug class

This medicine belongs to the Other general anesthetics class.

Drug family (ATC) Other general anesthetics
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

🏭 Manufacturer & labeler

LabelerNorco, Inc
FDA applicationNDA206009 (NDA)
Labeler code42602
First marketedSep 2008
Product typeHuman Prescription Drug
Portfolio3 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

🩺 Clinical

📗 Our plain-language guide HelloPharmacist
📖 Read our full Nitrous Oxide guide →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

🧪 Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

A current SPL was checked, but it does not contain a structured or narrative inactive-ingredient list for this product. This does not mean the product has no inactive ingredients.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

💲 Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer eachPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Try another pack size: 246 l 370 l 738 l 1599 l 2466 l 4920 l 7380 l 13800 l
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Nitrous Oxide 990 mL/L 10014-0003-10 Aero 774 l FDA listed
Nitrous Oxide 99 L/100L 10167-0200-01 Air 368 l FDA listed
Nitrous Oxide 99 L/100L 12121-0002-03 Badger 4920 l FDA listed
Nitrous Oxide 990 mL/L 12213-0593-13 NEXAIR, 986 l FDA listed
Nitrous Oxide 990 mL/L 17575-0011-01 AGL 12320 l FDA listed
Nitrous Oxide 990 mL/L 20703-0003-01 General 13798 l FDA listed
Nitrous Oxide 990 mL/L 22557-0003-01 AGP 265 l FDA listed
Nitrous Oxide 99 L/100L 24312-0003-01 Airtec 1477 l FDA listed
Nitrous Oxide 990 mL/L 34057-0010-01 Oxarc, 906 l Discontinued
Nitrous Oxide 99 L/100Lthis 42602-0003-09 Norco, 3700 l FDA listed
Nitrous Oxide 990 mL/L 42751-1075-01 FULLERTON 14163 l FDA listed
Nitrous Oxide 990 mL/L 43621-0003-11 DJB 198 l FDA listed
Nitrous Oxide 990 mL/L 44076-0012-01 American 160 l FDA listed
Nitrous Oxide 99 L/100L 44517-0020-01 Corrigan 940 l FDA listed
Nitrous Oxide 990 mL/L 46123-0006-01 Roberts 247 l FDA listed
Nitrous Oxide 990 mL/L 46123-0007-01 Roberts 91453 l FDA listed
Nitrous Oxide 99 L/100L 48273-0002-04 Keen 1632 l FDA listed
Nitrous Oxide 990 mL/L 49575-0003-01 Machine 2978 l FDA listed
Nitrous Oxide 990 mL/L 50554-0005-11 DuPuy 226 l FDA listed
Nitrous Oxide 990 mL/L 51486-0007-01 ILMO 15770 l Discontinued
Nitrous Oxide 99 L/100L 52568-0002-01 Crumpton 940 l FDA listed
Nitrous Oxide 99 L/100L 53511-0003-01 Volunteer 671 l FDA listed
Nitrous Oxide 99 kg/100kg 54218-0800-01 United 1.814 kg FDA listed
Nitrous Oxide 990 mL/L 54260-0001-01 Nitrous 8993600 l FDA listed
Nitrous Oxide 99 kg/100kg 55050-0018-01 Holston 2.9 kg FDA listed
Nitrous Oxide 990 mL/L 55404-0002-01 Lessors, 242 l FDA listed
Nitrous Oxide 990 mL/L 59579-0004-01 Linde 17987 l FDA listed
Nitrous Oxide 99 L/100L 62097-0004-01 Boggs 682 l FDA listed
Nitrous Oxide 990 mL/L 62273-0005-01 Metro 15770 l FDA listed
Nitrous Oxide 990 mL/L 63978-0201-01 Quality 2 l FDA listed
Nitrous Oxide 990 mL/L 67477-0002-01 MAVERICK 12300 l FDA listed
Nitrous Oxide 99 L/100L 67525-0400-01 Spectrum 1482 l FDA listed
Nitrous Oxide 990 mL/L 70151-0004-01 Central 532 l Discontinued
Nitrous Oxide 990 mL/L 72276-0002-01 MITCHELL 29.03 l FDA listed
About this product: this is the brand-name version. We did not find an FDA-approved generic match for this exact strength, form and route.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2008
On the market since
Sep 2008
📍
2026
Currently FDA-listed
18 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

🔬 Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Nitrous Oxide — the ingredient across all brands.

Top reported reactions

Drug Abuse136
Drug Interaction133
Cardiac Arrest121
Anaesthetic Complication Neurological117
Bradycardia101
Hypotension93
Subacute Combined Cord Degeneration84

Age at onset

Neonate24
Infant6
Child113
Adolescent6
Adult62
Elderly19

Reporter sex

2,188 reports
Male · 50%
Female · 49%
Unknown · 2%

Serious outcomes

Hospitalization828
Life-threatening325
Death222
Disabling68
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 149 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
42602-0003-01 1599 L in 1 CYLINDER (42602-003-01) 2008-09-01 Active
42602-0003-02 4920 L in 1 CYLINDER (42602-003-02) 2008-09-01 Active
42602-0003-03 13800 L in 1 CYLINDER (42602-003-03) 2008-09-01 Active
42602-0003-04 246 L in 1 CYLINDER (42602-003-04) 2008-09-01 Active
42602-0003-05 7380 L in 1 CYLINDER (42602-003-05) 2008-09-01 Active
42602-0003-06 738 L in 1 CYLINDER (42602-003-06) 2008-09-01 Active
42602-0003-07 2466 L in 1 CYLINDER (42602-003-07) 2008-09-01 Active
42602-0003-08 370 L in 1 CYLINDER (42602-003-08) 2008-09-01 Active
42602-0003-09 You're viewing this 3700 L in 1 CYLINDER (42602-003-09) 2008-09-01 Active

You're viewing one of 9 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 42602-0003-09?
NDC 42602-0003-09 contains 3700 l — 3700 l in 1 cylinder.
What is the difference between NDC 42602-0003-09 and NDC 42602-0003-04?
Both are NITROUS OXIDE 99 L/100L Gas — the drug itself is identical. NDC 42602-0003-09 is the 3700 l package, while NDC 42602-0003-04 is the 246 l package.
What NDC number is used to bill for this package of NITROUS OXIDE 99 L/100L Gas?
Bill NDC 42602-0003-09 — the 11-digit billing format is 42602000309. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 About this NDC listing & data coverage

Finished prescription product
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is available.
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 42602-003-09, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 42602-0003-09, written without dashes as 42602000309. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 42602-0003-09, the first segment (42602) is the labeler code FDA assigned to Norco, Inc; the middle segment (0003) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (09) identifies this exact package size and type. Together they name one specific package of one specific product.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Norco, Inc. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 8 other package presentations of this same product, including 246 l (42602-0003-04), 370 l (42602-0003-08), 738 l (42602-0003-06). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Norco, Inc is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as a prescription product, so it is dispensed under a prescriber's order. Your pharmacist can tell you whether any over-the-counter forms of the same medication exist.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.

📄 Full prescribing information FDA SPL

The complete FDA label for this product — the official prescribing information, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
📄 FDA label 9 words

No readable label sections were found for this product.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.