Oxygen

Oxygen

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

Company

DUNS: 087089350

Effective Date

October 9, 2009

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

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.

DUNS Number

087089350

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

Labeler

Apollo Services Inc.

Registrant

Apollo Services Inc.

DUNS Number

087089350

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

NDC Product Code

24781-0001

Route of Administration

RESPIRATORY (INHALATION)

Effective Date

October 9, 2009

Ingredients

Code: S88TT14065Class: ACTIBQuantity: 99 L in 100 L