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FDA Approval

OXYGEN

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

FDA Approval Summary

Company
Effective Date
October 18, 2023
Labeling Type
HUMAN PRESCRIPTION DRUG LABEL
Oxygen(99 L in 100 L)

Registrants1

Companies and organizations registered with the FDA for this drug approval, including their contact information and regulatory details.

MID-SOUTH WELDING SUPPLY, INC.

095705448

Manufacturing Establishments1

FDA-registered manufacturing facilities and establishments involved in the production, packaging, or distribution of this drug product.

MID-SOUTH WELDING SUPPLY, INC.

MID-SOUTH WELDING SUPPLY, INC.

MID-SOUTH WELDING SUPPLY, INC.

095705448

Products1

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

OXYGEN

Product Details

NDC Product Code
51400-001
Application Number
NDA205767
Marketing Category
NDA (C73594)
Route of Administration
RESPIRATORY (INHALATION)
Effective Date
October 18, 2023
OxygenActive
Code: S88TT14065Class: ACTIBQuantity: 99 L in 100 L
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