MedPath

Air

Air-Human

Approved
Approval ID

12b77ee5-bc4d-4f62-a98e-facd4ae7505a

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Nov 16, 2023

Manufacturers
FDA

Praxair Distribution, Inc.

DUNS: 042845636

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Air

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code59579-006
Application NumberNDA205910
Product Classification
M
Marketing Category
C73594
G
Generic Name
Air
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateNovember 16, 2023
FDA Product Classification

INGREDIENTS (1)

AIRActive
Quantity: 1000 mL in 1 L
Code: K21NZZ5Y0B
Classification: ACTIB

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Air - FDA Drug Approval Details