NDC 73705-002 Nitrogen


NDC Product Code 73705-002

NDC 73705-002-01

Package Description: 160 L in 1 CYLINDER

NDC 73705-002-02

Package Description: 180 L in 1 CYLINDER

NDC Product Information

Nitrogen with NDC 73705-002 is a a human prescription drug product labeled by Mjb Welding Supply, Inc.. The generic name of Nitrogen is nitrogen. The product's dosage form is gas and is administered via respiratory (inhalation) form.

Labeler Name: Mjb Welding Supply, Inc.

Dosage Form: Gas - Any elastic aeriform fluid in which the molecules are separated from one another and so have free paths.

Product Type: Human Prescription Drug What kind of product is this?
Indicates 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.

Nitrogen Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • NITROGEN 99 L/100L

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Respiratory (inhalation) - Administration within the respiratory tract by inhaling orally or nasally for local or systemic effect.
  • Respiratory (inhalation) - Administration within the respiratory tract by inhaling orally or nasally for local or systemic effect.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Mjb Welding Supply, Inc.
Labeler Code: 73705
FDA Application Number: NDA205766 What is the FDA Application Number?
This 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.

Marketing Category: NDA - A product marketed under an approved New Drug Application. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 03-01-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Nitrogen Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Mjb Nitrogen, Refrigerated

  • NITROGEN, REFRIGERATED LIQUID NF UN1977Rx onlyWARNINGAdministration of Nitrogen may be hazardous or contraindicated. For use only by or under the supervision of a licensed practitioner who is experienced in the use and administration of Nitrogen and is familiar with the indications, effects, dosages, methods, and frequency and duration of administration, and with the hazards, contraindications, and side effects, and the precautions to be taken.WARNINGCONTAINS REFRIGERATED GAS; MAY CAUSE CRYOGENIC BURNS OR INUURY.MAY DISPLACE OXYGEN AND CAUSE RAPID SUFFOCATION.Do not handle until all safety precautions have been read and understood. Use and store only outdoors or in a well-ventilated place. Wear cold insulating gloves, face shield, and eye protection. Use a back flow preventive device in the piping. DO NOT change or force fit connections.NON-FLAMMABLE GAS2Close valve after each use and when empty.Always keep container in upright position.Read and follow the Safety Data Sheet (SDS) before use.FIRST AID:IF INHALED: Remove person to fresh air and keep comfortable for breathing.IF ON SKIN: Thaw frosted parts with lukewarm water. Do not rub affected area. Get immediate medical advice/attention.CAS: 7727-37-9MJB                              357 EAST PARK AVENUE • P.O. BOX 2166WELDING SUPLY      CHICO, CA 95927                                        530-342-3589 • FAX 530-342-1715SECURE ALL CYLINDERS WHILE IN STORAGE AND IN USE.DO NOT REMOVE THIS PRODUCT LABEL.LABEL SOLUTINS, INC. • 1-800-296-9080 • 86387 (10/18)PN: 86387G-24-28

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