58632-003 NDC - AIR

Drug Information

  • Product NDC: 58632-003
  • Proprietary Name: Air
  • Non Proprietary Name: Air
  • Active Ingredient(s): 1000 mL/L AIR
  • Administration Route(s): RESPIRATORY (INHALATION)
  • Dosage Form(s): GAS

Labeler Information

Field Name Field Value
Labeler Name: GIBBS WELDING SUPPLY, INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA205859
Marketing Category: NDA
Start Marketing Date:10/12/2020

Package Information

No. Package Code Package Description Billing Unit
158632-003-01708 L in 1 CYLINDER (58632-003-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC58632-003The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN PRESCRIPTION DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEAirThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAirThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEGASThe translation of the dosage form Code submitted by the firm.
ROUTE NAMERESPIRATORY (INHALATION)The translation of the dosage form Code submitted by the firm.
START MARKETING DATE10/12/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMENDAThis is the date that the labeler indicates was the start of its marketing of the drug product.
APPLICATION NUMBERNDA205859This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEGIBBS WELDING SUPPLY, INC.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEAIRAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH1000 
ACTIVE INGRED UNITmL/L 

Download Record

Download this NDC record record in Text format: Export

Download this NDC record record in Excel (CSV) format: Export

Download this NDC record record in XML format: Export

This page was last updated on: 11/21/2025