# Oxygen

NDC: 50063-001
Generic name: Oxygen
Labeler / Manufacturer: Andy-Oxy Co., Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: GAS
Routes: RESPIRATORY (INHALATION)
Marketing started: 20070101

FDA application: NDA205767

## Active ingredients

- OXYGEN: 995 mL/L

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50063-001"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50063-001
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=265e287a-1dca-4f5b-98db-c98be97bc811