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Oxygen

Prescription NDA
Informational index, not medical advice. Content is reproduced from public FDA and NLM data. Always confirm against the manufacturer's current prescribing information. Report adverse events to FDA MedWatch.

Overview

Brand name
Oxygen
Generic name
Oxygen
Dosage form
Liquid
Route
Respiratory (Inhalation)
Marketing category
—
Labeler
BayCare Home Care, Inc.
Product type
Human Prescription Drug
DEA schedule
Not scheduled
Active ingredients
2
NDC product codes
2
Packages
7
Data completeness
46% of corroborating sources present

Active ingredients

Source: NDC Directory
Active ingredients and strengths as listed in the NDC Directory.
Ingredient Strength RxCUI Monograph
Oxygen 1000 g/L 312172 View
Oxygen 210 mg/kg 312172 View

Forms, strengths and routes

Source: NDC Directory
Dosage form
Liquid
Route of administration
Respiratory (Inhalation)
Presentations
9

Regulatory status

Source: Drugs@FDANDC Directory
Application number
205889
Application type
NDA · New Drug Application
Approval date
August 2, 2013
Sponsor
MATHESON TRI-GAS INC
Products on application
1
Submissions recorded
1
Products approved under application 205889.
Product Trade name Form Strength Ingredient Status TE Flags
205889-001 OXYGEN, USP GAS OXYGEN Prescription —

Approval history

Source: Drugs@FDA
Most recent submissions on application 205889.
Type No. Action Status Date Review
Original application 1 Medical Gas Approved August 2, 2013 Standard

Review documents

  • 0 · Original application · September 29, 2015

Adverse event reports

Source: openFDA FAERS
48,982
FAERS reports mentioning this drug
as of 2026-09-25T03:42:24+00:00
A report count is not a risk measure. FAERS accepts voluntary and mandatory reports without establishing causation, and reporting is influenced by how widely a drug is used, how long it has been marketed, and media attention. FDA states that reports “do not prove that the drug caused the event”. Compare rates, not totals.

Attributed to this product's most-reported active ingredient: OXYGEN. Combination products with more than six active ingredients are not attributed, because a report count summed across a long ingredient list measures the list, not the medicine.

Packaging and NDCs

Source: NDC Directory
Every National Drug Code package associated with this medication. The NDC is the identifier used for dispensing, billing and pharmacovigilance in the United States.
Package NDC Product NDC Labeler Description Marketing start
62137-001-00 62137-001 AMO Medical Oxygen, Inc. 31 L in 1 DEWAR (62137-001-00) May 1, 1995
62137-001-01 62137-001 AMO Medical Oxygen, Inc. 200 L in 1 DEWAR (62137-001-01) May 1, 1995
62137-001-02 62137-001 AMO Medical Oxygen, Inc. 291 L in 1 DEWAR (62137-001-02) May 1, 1995
59400-005-05 59400-005 BayCare Home Care, Inc. 22.68 kg in 1 DEWAR (59400-005-05) January 13, 2025
59400-005-06 59400-005 BayCare Home Care, Inc. 34.02 kg in 1 DEWAR (59400-005-06) January 13, 2025
59400-005-07 59400-005 BayCare Home Care, Inc. 45.36 kg in 1 DEWAR (59400-005-07) January 13, 2025
59400-005-08 59400-005 BayCare Home Care, Inc. 49.9 kg in 1 DEWAR (59400-005-08) January 13, 2025
62137-001 62137-001 AMO Medical Oxygen, Inc. — May 1, 1995
59400-005 59400-005 BayCare Home Care, Inc. — September 23, 2022

Sources for this page

Every dataset that contributed a fact to this page.
Dataset Agency Used for
NDC Directory FDA Identity, ingredients, strengths, forms, routes, labelers, packages
Drugs@FDA FDA Application, sponsor, submissions, review documents, marketing status
FAERS FDA Adverse event report counts

Generated September 25, 2026 · 9 sections on this page.