nitrous oxide

Generic: nitrous oxide

Labeler: nitrous oxide
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name nitrous oxide
Generic Name nitrous oxide
Labeler nitrous oxide
Dosage Form GAS
Routes
RESPIRATORY (INHALATION)
Active Ingredients

nitrous oxide 990 mL/L

Manufacturer
Nitrous Oxide

Identifiers & Regulatory

Product NDC 54260-001
Product ID 54260-001_4358f26d-144b-9a1d-e063-6394a90ac2b5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA206009
Listing Expiration 2026-12-31
Marketing Start 2000-01-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 54260001
Hyphenated Format 54260-001

Supplemental Identifiers

RxCUI
312022
UNII
K50XQU1029

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name nitrous oxide (source: ndc)
Generic Name nitrous oxide (source: ndc)
Application Number NDA206009 (source: ndc)
Routes
RESPIRATORY (INHALATION)
source: ndc

Resolved Composition

Strengths
  • 990 mL/L
source: ndc
Packaging
  • 8993600 L in 1 CYLINDER (54260-001-01)
source: ndc

Packages (1)

Ingredients (1)

nitrous oxide (990 mL/L)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "4358f26d-144b-9a1d-e063-6394a90ac2b5", "openfda": {"unii": ["K50XQU1029"], "rxcui": ["312022"], "spl_set_id": ["2b0b9cc4-fca7-4e84-8d9d-0f9852528579"], "manufacturer_name": ["Nitrous Oxide"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "8993600 L in 1 CYLINDER (54260-001-01)", "package_ndc": "54260-001-01", "marketing_start_date": "20000101"}], "brand_name": "Nitrous Oxide", "product_id": "54260-001_4358f26d-144b-9a1d-e063-6394a90ac2b5", "dosage_form": "GAS", "product_ndc": "54260-001", "generic_name": "Nitrous Oxide", "labeler_name": "Nitrous Oxide", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nitrous Oxide", "active_ingredients": [{"name": "NITROUS OXIDE", "strength": "990 mL/L"}], "application_number": "NDA206009", "marketing_category": "NDA", "marketing_start_date": "20000101", "listing_expiration_date": "20261231"}