MedPath
FDA Approval

OXYGEN

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

FDA Approval Summary

Company
Ctws, LLC
DUNS: 070941877
Effective Date
October 15, 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.

Ctws, LLC

070941877

Manufacturing Establishments1

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

Ctws, LLC

Ctws, LLC

Ctws, LLC

070941877

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
14208-532
Application Number
NDA205767
Marketing Category
NDA (C73594)
Route of Administration
RESPIRATORY (INHALATION)
Effective Date
January 1, 2018
OxygenActive
Code: S88TT14065Class: ACTIBQuantity: 99 L in 100 L
© Copyright 2025. All Rights Reserved by MedPath