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Nitrogen

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Active ingredient
Nitrogen 990 mL/1 L
Other brand names
Dosage form
Gas
Route
Respiratory (inhalation)
Prescription status
Rx (prescription)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2018
Label revision date
November 21, 2025
FDA Insert
Prescribing information, PDF file
Active ingredient
Nitrogen 990 mL/1 L
Other brand names
Dosage form
Gas
Route
Respiratory (inhalation)
Prescription status
Rx (prescription)
CSA schedule
Not a scheduled drug
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2018
Label revision date
November 21, 2025
Manufacturer
FULLERTON WELDING SUPPLY
Registration number
NDA205866
NDC root
42751-1074
FDA Insert
Prescribing information, PDF file
Packaging Info (7 NDCs)
Packaging & NDC Codes (7)

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

If you are a consumer or patient please visit this version.

Drug Overview

Nitrogen NF is a highly purified form of nitrogen gas, with a purity specification of 99.999 percent. It is primarily used in medical applications, particularly by healthcare providers who are registered with the FDA. This product is odorless and has been rigorously tested to ensure it meets strict quality standards, making it suitable for various medical uses.

In medical settings, nitrogen can serve multiple purposes, including providing an inert atmosphere for certain procedures and applications. Its high purity ensures that it does not introduce contaminants that could affect patient safety or the efficacy of medical treatments.

Uses

You should know that this product is intended for use in specific medical applications and is only available to medical customers who are properly registered with the FDA. This means that it is designed for professional use in healthcare settings rather than for personal use at home.

Additionally, there are no reported teratogenic effects (which means it does not cause birth defects) or nonteratogenic effects associated with this product. This information is important for understanding the safety profile of the drug in various contexts.

Dosage and Administration

When using this medication, you will administer it through your respiratory system by inhalation (breathing it in). The dosage you need to use is 990 mL of nitrogen in a total volume of 1 liter.

Make sure to follow the instructions carefully to ensure you are using the correct amount. If you have any questions about how to use this medication or its effects, don’t hesitate to reach out to your healthcare provider for guidance.

What to Avoid

There are no specific contraindications, controlled substance classifications, or concerns regarding abuse, misuse, or dependence associated with this medication. This means that, based on the available information, there are no particular situations or conditions under which you should avoid using it. Always consult with your healthcare provider for personalized advice and to ensure that this medication is appropriate for your individual health needs.

Side Effects

There are no known side effects or adverse reactions associated with the use of nitrogen gas as a human prescription drug. The information available focuses solely on product details and specifications, without any mention of potential negative effects. If you have any concerns or experience unusual symptoms, it's always best to consult with your healthcare provider.

Warnings and Precautions

While there are no specific warnings or precautions listed for this medication, it's always important to stay informed about your health. If you experience any unusual symptoms or have concerns while using this medication, it's a good idea to consult your doctor for guidance.

Since there are no required lab tests or emergency instructions provided, you can feel reassured that this medication does not have additional monitoring needs. However, if you ever feel uncertain about your treatment or notice any changes in your health, don't hesitate to reach out to your healthcare provider for advice. Your well-being is the top priority.

Overdose

It appears that there is no specific information available regarding overdosage for this medication. However, it's always important to be aware of the signs of an overdose, which can include symptoms like extreme drowsiness, confusion, or difficulty breathing. If you suspect that you or someone else may have taken too much of a medication, it’s crucial to seek immediate medical help.

In case of an overdose, you should contact your local emergency services or go to the nearest hospital right away. Having the medication packaging or information on hand can help medical professionals provide the best care. Always remember that when it comes to medications, it's better to be safe and get help if you have any concerns.

Pregnancy Use

When it comes to using this medication during pregnancy, there is no specific information available about its safety, recommended dosage adjustments, or any special precautions you should take. This means that if you are pregnant or planning to become pregnant, it’s important to consult with your healthcare provider before starting or continuing this medication. They can help you weigh the potential risks and benefits based on your individual situation. Always prioritize open communication with your doctor to ensure the best care for you and your baby.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to know that there is no specific information available regarding the safety or effects of this medication on nursing mothers or their infants. Since there are no guidelines or data provided, it’s advisable to consult your healthcare provider for personalized advice. They can help you weigh the benefits and risks based on your individual situation. Always prioritize your health and your baby's well-being when making decisions about medication during breastfeeding.

Pediatric Use

Currently, there is no specific information available regarding the use of this medication in children. This means that the safety and effectiveness of the drug for pediatric patients (children and adolescents) have not been established. If you are considering this medication for a child, it is essential to consult with a healthcare professional for guidance and to discuss any potential risks or alternatives. Always prioritize your child's health and well-being by seeking expert advice.

Geriatric Use

When it comes to using this medication in older adults, there is no specific information available about dosage adjustments, safety concerns, or special precautions. This means that if you or a loved one is an older adult, it’s important to consult with a healthcare provider for personalized advice. They can help determine the best approach based on individual health needs and any other medications being taken. Always prioritize open communication with your healthcare team to ensure safe and effective treatment.

Renal Impairment

It appears that there is no specific information available regarding dosage adjustments, monitoring, or safety considerations for patients with kidney problems. This means that if you have renal impairment (kidney issues), you should consult your healthcare provider for personalized advice. They can help determine the best course of action based on your individual health needs and any medications you may be taking. Always prioritize open communication with your doctor about your kidney health to ensure safe and effective treatment.

Hepatic Impairment

If you have liver problems, it's important to know that there are no specific guidelines or dosage adjustments mentioned for your condition in the available information. This means that the standard recommendations for the medication do not change based on liver function. However, it’s always a good idea to discuss your liver health with your healthcare provider, as they can offer personalized advice and monitor your condition appropriately.

Make sure to keep your doctor informed about any liver issues you may have, as they can help ensure that your treatment is safe and effective for you.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications or tests you may be taking. While there are no specific drug interactions or laboratory test interactions noted for this medication, your healthcare provider can help ensure that everything you are taking works well together and is safe for you.

Always feel free to ask questions and share your complete list of medications and any lab tests you may be undergoing. This way, you can receive the best possible care tailored to your needs.

Storage and Handling

To ensure the best care for your product, store it in a DEWAR container, which is a specialized vessel designed to keep materials at very low temperatures. It's important to use a DEWAR that is not a combination type, as this can affect the integrity of the storage. While there is no specific temperature range provided for storage, handling the DEWAR with care is crucial to prevent any damage.

When using the DEWAR, always be mindful of its condition and avoid any rough handling. This will help maintain the safety and effectiveness of the product. If you need to dispose of the DEWAR or its contents, follow local regulations for safe disposal.

Additional Information

You will use this medication through inhalation, which means you will breathe it in to receive the treatment. There are no additional details available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experiences related to this medication.

FAQ

What is the general description of Nitrogen NF?

Nitrogen NF is a product that has been tested for indicated parameters and meets the contractually guaranteed purity specifications.

What are the specifications for Nitrogen NF?

Nitrogen NF has a specification limit of ≥ 99.999 percent nitrogen, ≤ 5.00 ppm oxygen, and no odor.

What is the route of administration for Nitrogen NF?

Nitrogen NF is administered via respiratory (inhalation).

What is the dosage for Nitrogen NF?

The dosage for Nitrogen NF is 990 mL in 1 L.

Are there any contraindications for using Nitrogen NF?

No contraindications are listed for Nitrogen NF.

What should I know about the storage of Nitrogen NF?

Store Nitrogen NF in a DEWAR container, ensuring it is not a combination type, and handle with care to avoid damage.

Is there any information on the use of Nitrogen NF during pregnancy?

No specific information regarding the use of Nitrogen NF during pregnancy is provided.

What are the indications for using Nitrogen NF?

Nitrogen NF is indicated for use in medical applications by customers properly registered with the FDA.

Who released Nitrogen NF and when?

Nitrogen NF was released by Kevin N. Shue on 8/16/2018 at 9:43 AM.

Packaging Info

The table below lists all NDC Code configurations of Nitrogen, the U.S. brand-name prescription product. Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Nitrogen.
Details

FDA Insert (PDF)

This is the full prescribing document for Nitrogen, submitted to the U.S. Food and Drug Administration (FDA). It contains official information for healthcare providers, including how to use the medication, possible side effects, and safety warnings.

View FDA-approved insert (PDF)

Description

No description information is available for the specified drug.

Uses and Indications

This drug is indicated for use in medical applications by healthcare professionals and medical customers who are properly registered with the FDA.

Limitations of Use: The indications for this drug are strictly applicable within the context of medical use, and it is not intended for non-medical applications. There are no reported teratogenic or nonteratogenic effects associated with this drug.

Dosage and Administration

The medication is administered via the respiratory route through inhalation. The recommended dosage is 990 mL of nitrogen in a total volume of 1 liter.

Healthcare professionals should ensure that the preparation is conducted in a controlled environment, adhering to all safety protocols for handling gases. The administration should be performed using appropriate inhalation devices to ensure effective delivery to the patient.

Contraindications

There are no contraindications associated with the use of this product. It is not classified as a controlled substance, and there are no known risks of abuse, misuse, or dependence.

Warnings and Precautions

There are currently no specific warnings or precautions associated with the use of this medication. Healthcare professionals should be aware that no particular laboratory tests are required or suggested for safe use. Additionally, there are no defined instructions for patients regarding when to seek emergency medical help or when to discontinue use and contact their healthcare provider. It is essential for healthcare professionals to remain vigilant and monitor patients for any unforeseen reactions or complications, despite the absence of outlined warnings and precautions.

Side Effects

There are no reported adverse reactions associated with the use of nitrogen gas as a human prescription drug. The available information primarily consists of product details, manufacturing specifications, and related data, without any mention of side effects or adverse reactions in clinical trials or postmarketing experiences. As such, healthcare professionals should be aware that no specific adverse reactions have been documented for this product.

Drug Interactions

There are currently no documented drug interactions associated with this medication. Additionally, there are no known interactions with laboratory tests. As such, no specific recommendations for dosage adjustments or monitoring are warranted at this time.

Packaging & NDC

The table below lists all NDC Code configurations of Nitrogen, the U.S. brand-name prescription product. Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Nitrogen.
Details

Pediatric Use

No pediatric use information is provided in the insert. Therefore, the safety and efficacy of this medication in pediatric patients have not been established. Healthcare professionals should exercise caution when considering this treatment for children, infants, or adolescents, as there are no available data to guide dosing or therapeutic outcomes in these populations.

Geriatric Use

There is no specific information regarding the use of this medication in geriatric patients, including dosage adjustments, safety concerns, or special precautions. Healthcare providers should exercise caution when prescribing this medication to elderly patients, as individual responses may vary. It is advisable to monitor these patients closely for any adverse effects or changes in efficacy.

Pregnancy

There is no specific information available regarding the use of this medication during pregnancy, including safety concerns, dosage modifications, or special precautions that should be taken. Healthcare professionals are advised to consider the lack of data when prescribing this medication to pregnant patients and to weigh the potential benefits against any unknown risks to fetal outcomes. Women of childbearing potential should be counseled accordingly.

Lactation

There is no relevant information regarding nursing mothers or lactation considerations available in the provided text. Therefore, the effects of this medication on breastfed infants and its excretion in breast milk remain undetermined. Healthcare professionals should exercise caution and consider the potential risks and benefits when prescribing this medication to lactating mothers.

Renal Impairment

There is no information available regarding renal impairment, dosage adjustments, special monitoring, or safety considerations for patients with reduced kidney function. Healthcare professionals should exercise caution and consider individual patient circumstances when prescribing this medication to patients with renal impairment.

Hepatic Impairment

There is no information available regarding the use of this medication in patients with hepatic impairment. Consequently, there are no dosage adjustments, special monitoring requirements, or precautions specified for individuals with compromised liver function. Healthcare professionals should exercise caution and consider the individual patient's liver status when prescribing this medication.

Overdosage

In the absence of specific overdosage information, it is essential for healthcare professionals to remain vigilant regarding the potential for overdose with this medication. In cases where an overdose is suspected, immediate medical attention should be sought.

Healthcare providers are advised to monitor patients closely for any signs or symptoms that may arise from an overdose. Common symptoms may include, but are not limited to, severe drowsiness, confusion, respiratory distress, or any other unusual clinical manifestations.

Management of an overdose should be tailored to the individual patient and may involve supportive care, including monitoring vital signs and providing symptomatic treatment as necessary. In cases of significant overdose, consultation with a poison control center or a medical toxicologist is recommended to determine the most appropriate course of action.

It is crucial for healthcare professionals to educate patients about the importance of adhering to prescribed dosages and to provide guidance on what to do in the event of a suspected overdose.

Nonclinical Toxicology

No teratogenic or non-teratogenic effects have been reported in the available nonclinical studies. Additionally, there is no information regarding animal pharmacology and toxicology. The absence of data limits the assessment of potential risks associated with the compound in these areas.

Postmarketing Experience

No postmarketing experience details are available in the provided data.

Patient Counseling

Healthcare providers should advise patients that this product is intended exclusively for use in medical applications or by medical customers who are properly registered with the FDA. It is important for patients to understand that the product delivered has undergone testing for the indicated parameters and meets the contractually guaranteed purity specifications.

Providers should inform patients that the results provided are nominal values that fall within the statistical accuracy of the analytical test methods employed. Additionally, patients should be made aware that analysis on the storage tank is conducted periodically to ensure ongoing compliance with safety and quality standards. Each delivery unit is also subjected to analysis for specified parameters, reinforcing the commitment to quality and reliability in the product's use.

Storage and Handling

The product is supplied in a DEWAR container, which must not be of a combination type. It is essential to handle the DEWAR with care to prevent any damage. While no specific temperature range for storage is provided, the integrity of the DEWAR should be maintained to ensure optimal conditions for the product.

Additional Clinical Information

The route of administration for the medication is via respiratory inhalation. There are no additional details available regarding laboratory tests, abuse information, patient counseling, or postmarketing experience.

FDA Insert (PDF)

This document is the official FDA-approved prescribing information for Nitrogen as submitted by FULLERTON WELDING SUPPLY. It includes detailed information about indications, dosage, contraindications, warnings, and clinical pharmacology.

View full prescribing information (PDF)

Data Generation & Sources

This page was automatically generated and is maintained by the AllDrugs AI Data-Science Team. It was built from the FDA Structured Product Label (DailyMed) for Nitrogen, retrieved by a validated AI data-extraction workflow.

All FDA-approved dosage forms and strengths are listed in the Packaging & NDC Codes section above. Regulatory status, pharmacologic class (EPC), and mechanism of action (MoA) were cross-checked against the FDA Orange Book (NDA205866) and the NSDE NDC Directory daily file.

Note: an automated daemon monitors NSDE checksums; when the record for this NDC changes, the new file is pulled instantly and this page is refreshed.

No human clinician has reviewed this version.

Learn more in our Editorial Policy

Last AI update:

Primary FDA sources:

Orange Book data shown on this page are limited to Regulatory Status (Rx), Established Pharmacologic Class (EPC), and Mechanism of Action (MoA).

Regulatory data notice: Information on this page is reproduced verbatim from FDA public databases (NSDE, Orange Book, Purple Book, DailyMed SPL). NDA/ANDA drugs are FDA-approved, BLA biologics are FDA-licensed. Inclusion alone does not guarantee current market availability or imply FDA endorsement.

Medical disclaimer: This AI-generated content is provided for educational purposes only and does not constitute medical advice. Always consult a licensed healthcare professional for diagnosis or treatment decisions.