Label: OXYGEN gas
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Contains inactivated NDC Code(s)
NDC Code(s): 10671-013-60, 10671-013-61 - Packager: Air Liquide America L.P.
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Drug Application
Drug Label Information
Updated February 19, 2015
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- OXYGEN USP CERTIFICATE OF ANALYSIS
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INGREDIENTS AND APPEARANCE
OXYGEN
oxygen gasProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:10671-013 Route of Administration RESPIRATORY (INHALATION) Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OXYGEN (UNII: S88TT14065) (OXYGEN - UNII:S88TT14065) OXYGEN 99 L in 100 L Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10671-013-60 25000 L in 1 TANK 2 NDC:10671-013-61 50000 L in 1 TANK Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA205827 01/01/1960 Labeler - Air Liquide America L.P. (003312600) Registrant - Air Liquide America L.P. (003312600) Establishment Name Address ID/FEI Business Operations Air Liquide America L.P. 831996405 manufacture(10671-013)
