NDC 10671-101

EZ-OX Plus

Ez-ox Plus

EZ-OX Plus is a Respiratory (inhalation) Gas in the Human Prescription Drug category. It is labeled and distributed by Air Liquide America L.p.. The primary component is Oxygen.

• Product ID: 10671-101_5e617966-03e2-48f3-b2f9-b5a48087dd54
• NDC: 10671-101
• Product Type: Human Prescription Drug
• Proprietary Name: EZ-OX Plus
• Generic Name: Ez-ox Plus
• Dosage Form: Gas
• Route of Administration: RESPIRATORY (INHALATION)
• Marketing Start Date: 1960-01-01
• Marketing Category: NDA / NDA
• Application Number: NDA205827
• Labeler Name: Air Liquide America L.P.
• Substance Name: OXYGEN
• Active Ingredient Strength: 99 L/100L
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 10671-101-04

708 L in 1 CYLINDER (10671-101-04)

• Marketing Start Date: 1960-01-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 10671-101-04 [10671010104]

EZ-OX Plus GAS

• Marketing Category: NDA
• Application Number: NDA205827
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1960-01-01
• Inactivation Date: 2019-11-27

Drug Details

Active Ingredients

Ingredient	Strength
OXYGEN	99 L/100L

OpenFDA Data

• SPL SET ID: d679680a-baf6-462a-9e13-319a52578ff5
• Manufacturer:
  • Air Liquide America L.P.
• UNII:
  • S88TT14065
• RxNorm Concept Unique ID - RxCUI:
  • 312172