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FDA Approval

OXYGEN

CompanyNorco, Inc. (DUNS: 043694645)

Effective Date

November 23, 2023

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Oxygen(999 L in 1000 L)

Registrants (1)

DUNS Number

043694645

Manufacturing Establishments (2)

Labeler

Norco, Inc.

Registrant

Norco, Inc.

DUNS Number

034050950

Labeler

Norco, Inc.

Registrant

Norco, Inc.

DUNS Number

081037862

Products (1)

OXYGEN

NDC Product Code

42602-001

Application Number

NDA205820

Marketing Category

NDA (C73594)

Route of Administration

RESPIRATORY (INHALATION)

Effective Date

November 23, 2023

Ingredients

OxygenActive

Code: S88TT14065Class: ACTIBQuantity: 999 L in 1000 L

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