nitrous oxide

Generic: nitrous oxide

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

Drug Facts

Product Profile

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

nitrous oxide 900 mL/L

Manufacturer
Nitrous Oxide of Canada

Identifiers & Regulatory

Product NDC 72343-001
Product ID 72343-001_435903ef-7e72-cff6-e063-6294a90af4d5
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 72343001
Hyphenated Format 72343-001

Supplemental Identifiers

RxCUI
347107
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
  • 900 mL/L
source: ndc
Packaging
  • 89936 L in 1 CYLINDER (72343-001-01)
source: ndc

Packages (1)

Ingredients (1)

nitrous oxide (900 mL/L)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "435903ef-7e72-cff6-e063-6294a90af4d5", "openfda": {"unii": ["K50XQU1029"], "rxcui": ["347107"], "spl_set_id": ["6cd11814-c704-1b74-e053-2991aa0a0619"], "manufacturer_name": ["Nitrous Oxide of Canada"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "89936 L in 1 CYLINDER (72343-001-01)", "package_ndc": "72343-001-01", "marketing_start_date": "20000101"}], "brand_name": "Nitrous Oxide", "product_id": "72343-001_435903ef-7e72-cff6-e063-6294a90af4d5", "dosage_form": "GAS", "product_ndc": "72343-001", "generic_name": "Nitrous Oxide", "labeler_name": "Nitrous Oxide of Canada", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nitrous Oxide", "active_ingredients": [{"name": "NITROUS OXIDE", "strength": "900 mL/L"}], "application_number": "NDA206009", "marketing_category": "NDA", "marketing_start_date": "20000101", "listing_expiration_date": "20261231"}