Label: NITROUS OXIDE gas
- NDC Code(s): 72343-001-01
- Packager: Nitrous Oxide of Canada
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Drug Application
Drug Label Information
Updated October 4, 2024
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INGREDIENTS AND APPEARANCE
NITROUS OXIDE
nitrous oxide gasProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72343-001 Route of Administration RESPIRATORY (INHALATION) Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NITROUS OXIDE (UNII: K50XQU1029) (NITROUS OXIDE - UNII:K50XQU1029) NITROUS OXIDE 900 mL in 1 L Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72343-001-01 89936 L in 1 CYLINDER; Type 0: Not a Combination Product 01/01/2000 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA206009 01/01/2000 Labeler - Nitrous Oxide of Canada (205078801) Registrant - Nitrous Oxide of Canada (205078801) Establishment Name Address ID/FEI Business Operations Nitrous Oxide of Canada 205078801 manufacture(72343-001)