Nitrous Oxide

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Nitrous Oxide
Generic name: NITROUS OXIDE
Manufacturer: Nitrous Oxide of Canada
Product type: HUMAN PRESCRIPTION DRUG
SPL set ID: 6cd11814-c704-1b74-e053-2991aa0a0619
SPL ID: 435903ef-7e72-cff6-e063-6294a90af4d5
Version: 9
Effective date: 2025-11-11
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:16:49

Harmonized routes table
Harmonized routes
RESPIRATORY (INHALATION)

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application applno	NDA	206009	derived:openfda.application_number
application number		NDA206009	openfda.application_number
brand name		Nitrous Oxide	openfda.brand_name
generic name		NITROUS OXIDE	openfda.generic_name
manufacturer name		Nitrous Oxide of Canada	openfda.manufacturer_name
ndc	package	72343-001-01	openfda.package_ndc
ndc	product	72343-001	openfda.product_ndc
ndc11	package	72343000101	derived:openfda.package_ndc
rxcui		347107	openfda.rxcui
spl id		435903ef-7e72-cff6-e063-6294a90af4d5	id
spl set id		6cd11814-c704-1b74-e053-2991aa0a0619	set_id
unii		K50XQU1029	openfda.unii

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