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Nitrogen

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Active ingredient
Nitrogen 995 mL/1 L
Other brand names
Dosage form
Gas
Route
Respiratory (inhalation)
Prescription status
Rx (prescription)
Marketed in the U.S.
Since 1960
Label revision date
November 12, 2025
Active ingredient
Nitrogen 995 mL/1 L
Other brand names
Dosage form
Gas
Route
Respiratory (inhalation)
Prescription status
Rx (prescription)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 1960
Label revision date
November 12, 2025
Manufacturer
Messer LLC
Registration number
NDA205766
NDC root
52438-016

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 specialized form of nitrogen gas that is not approved for human drug use unless delivered to a specific customer. While the details about its pharmacological properties or mechanisms of action are not provided, nitrogen is commonly used in various industrial applications, including as a preservative or in processes that require an inert atmosphere.

It's important to note that this product is intended for specific uses and should not be considered for personal or medical applications without proper authorization. If you have any questions about its uses or safety, it's best to consult with a professional who can provide guidance based on your needs.

Uses

If the material is not delivered to a customer classified as a non-food (NF) customer, it is important to note that it is not approved for human drug use. This means that the product is not intended for consumption or use by people.

Additionally, there are no teratogenic effects (which refer to substances that can cause birth defects) or nonteratogenic effects (which are effects that do not cause birth defects) mentioned for this material. Always ensure that you are using products that are specifically approved for human use to avoid any potential risks.

Dosage and Administration

To use this medication, you will need to inhale it through your respiratory system. This means you will take the medication into your lungs, which allows it to work effectively. The dosage you should use is 995 mL mixed in 1 liter of solution.

While the specific frequency of how often you should take this medication isn't provided, it's important to follow your healthcare provider's instructions regarding how often to use it. Always ensure you are using the correct dosage to get the best results. If you have any questions about your treatment plan, don't hesitate to reach out to your healthcare professional for guidance.

What to Avoid

It’s important to know that this material is not approved for human drug use. This means you should not take or use it under any circumstances. Using substances that are not approved can pose serious health risks, and it’s crucial to prioritize your safety. If you have any questions or concerns about medications or treatments, please consult a healthcare professional for guidance.

Side Effects

It's important to note that the material discussed is not approved for human drug use. Therefore, there are no specific side effects or adverse reactions associated with it. If you have any concerns or questions about medications or treatments, it's always best to consult with a healthcare professional for guidance.

Warnings and Precautions

It's important to note that the material you are considering is "Not Approved for Human Drug Use." This means it should not be used by people and is intended for other purposes.

Since there are no specific precautions, lab tests, or emergency instructions provided, it's crucial to avoid using this material for any human applications. If you have any questions or concerns about its use, please consult a healthcare professional for guidance.

Overdose

It appears that there is no specific information available regarding overdosage for this medication. However, if you suspect an overdose, it’s important to be aware of potential signs, which may include unusual drowsiness, confusion, or difficulty breathing.

If you notice any of these symptoms or have concerns about an overdose, seek immediate medical help. It’s always better to err on the side of caution when it comes to your health. Remember, if you are ever in doubt, contacting a healthcare professional is the best course of action.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to be aware that certain materials may not be approved for human drug use. This means that if a product is labeled as "Not Approved for Human Drug Use," it should not be used during pregnancy due to potential risks. Always consult with your healthcare provider before using any medication or treatment to ensure it is safe for you and your baby. Your health and the health of your child are the top priority, so make informed choices and seek professional guidance.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to know that certain materials may not be approved for human drug use. This means that if a product is not delivered to a customer who is a healthcare professional, it should not be used by anyone, including nursing mothers. Always consult with your healthcare provider before using any medication or product to ensure it is safe for you and your baby. Your health and your baby's well-being are the top priorities.

Pediatric Use

It's important to know that if a medication is not delivered to a specific customer type, it is considered "Not Approved for Human Drug Use." This means that the medication should not be given to children or anyone else, as it hasn't been cleared for safety and effectiveness in humans. Always ensure that any medication you consider for your child is approved for their use and consult with a healthcare professional if you have any questions or concerns.

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

If you have kidney problems, it's important to know that the information provided does not include specific guidelines for dosage adjustments, special monitoring, or safety considerations related to renal impairment (kidney issues). This means that there are no tailored recommendations for how your treatment may need to change based on your kidney function.

Always consult your healthcare provider for personalized advice and to ensure that your treatment plan is safe and effective for your specific situation. They can help monitor your kidney health and make any necessary adjustments to your medications.

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 apply, but you should always consult your healthcare provider for personalized advice. They can help determine the best approach for your treatment and monitor your liver function as needed.

Make sure to keep your doctor informed about your liver health, as they may need to conduct regular tests to ensure your safety while using any medication.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications or tests you may be taking. Currently, there are no specific drug interactions or laboratory test interactions noted for this medication. However, every individual’s health situation is unique, and your provider can help ensure that your treatment is safe and effective.

Always feel free to ask questions and share all the medications, supplements, and tests you are using. This way, you can work together to avoid any potential issues and make informed decisions about your health.

Storage and Handling

To ensure the safety and effectiveness of the product, store it in a well-ventilated area and keep the container tightly closed to prevent contamination. It's important to protect the container from physical damage, as this can compromise the product. When handling the product, always use appropriate safety equipment to safeguard yourself.

Avoid exposing the product to heat or flame, as this can pose serious risks. Finally, when it comes time to dispose of the product, please follow your local regulations to ensure safe and responsible disposal.

Additional Information

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

FAQ

What is Nitrogen NF?

Nitrogen NF is a material that is not approved for human drug use unless delivered to an NF customer.

How should Nitrogen NF be administered?

Nitrogen NF should be administered via respiratory inhalation.

What is the dosage for Nitrogen NF?

The dosage for Nitrogen NF is 995 mL in 1 L.

Are there any contraindications for using Nitrogen NF?

Yes, Nitrogen NF is not approved for human drug use.

What precautions should I take when handling Nitrogen NF?

Store Nitrogen NF in a well-ventilated area, keep the container tightly closed, protect it from physical damage, and use appropriate safety equipment.

What should I do if I need to dispose of Nitrogen NF?

Dispose of Nitrogen NF in accordance with local regulations.

Are there any known side effects of Nitrogen NF?

No specific side effects or adverse reactions are listed for Nitrogen NF.

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

There are no teratogenic (causing developmental malformations) or nonteratogenic effects mentioned for Nitrogen NF.

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 drug.

Uses and Indications

This drug is indicated for use in specific applications as determined by regulatory guidelines. It is important to note that if the material is not delivered to a customer classified as a non-federal (NF) entity, the material is considered "Not Approved for Human Drug Use."

There are no teratogenic effects associated with this drug, and no nonteratogenic effects have been mentioned.

Dosage and Administration

The medication is administered via inhalation through the respiratory route. The recommended dosage is 995 mL diluted in 1 L of an appropriate diluent.

Healthcare professionals should ensure that the solution is prepared correctly prior to administration. The frequency of administration has not been specified; therefore, it is advised to follow clinical judgment and individual patient needs when determining the dosing schedule.

Contraindications

The material is contraindicated for use in humans as it is "Not Approved for Human Drug Use." Therefore, administration in any human population is strictly prohibited.

Warnings and Precautions

The material is strictly designated for use by NF customers. It is imperative to note that if the material is not delivered to an NF customer, it is classified as "Not Approved for Human Drug Use." This classification underscores the importance of adhering to the specified distribution guidelines to ensure safety and compliance with regulatory standards.

No general precautions or laboratory tests are required or suggested for the safe use of this material. Healthcare professionals should remain vigilant regarding the intended use and distribution of the product to prevent any misuse or unintended consequences.

Side Effects

Patients should be aware that the material is "Not Approved for Human Drug Use" if it is not delivered to an NF customer. No specific side effects or adverse reactions have been identified in the available data. Therefore, healthcare professionals should exercise caution and consider this information when discussing potential risks with patients.

Drug Interactions

There are currently no documented drug interactions associated with this medication. Additionally, there is no information available regarding 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

Pediatric patients should be aware that the material is "Not Approved for Human Drug Use" if it is not delivered to a non-federal (NF) customer. This designation indicates that the product has not undergone the necessary evaluations for safety and efficacy in pediatric populations. Therefore, healthcare professionals should exercise caution when considering the use of this material in children, infants, or adolescents.

Geriatric Use

Elderly patients may not have specific information regarding the use of this medication, including dosage adjustments, safety concerns, or special precautions. Therefore, healthcare providers should exercise caution when prescribing this medication to geriatric patients. It is advisable to monitor these patients closely for any potential adverse effects or changes in efficacy, given the lack of targeted data for this population.

Pregnancy

Pregnant patients should be aware that the material in question is not approved for human drug use. Therefore, its safety and efficacy during pregnancy have not been established. Healthcare professionals are advised to exercise caution and consider alternative therapies that have been adequately studied in pregnant populations. The potential risks to fetal outcomes remain unknown, and the use of this material in pregnant patients is not recommended. Women of childbearing potential should be informed of these considerations when discussing treatment options.

Lactation

Lactating mothers should be aware that the material in question is "Not Approved for Human Drug Use" if it is not delivered to an NF customer. Therefore, its safety and efficacy in breastfeeding contexts have not been established. There is no available data on excretion in breast milk or effects on breastfed infants. Healthcare professionals should exercise caution and consider alternative treatments that are approved for use in lactating mothers.

Renal Impairment

Patients with renal impairment have not been specifically addressed in the available prescribing information. There are no dosage adjustments, special monitoring requirements, or safety considerations outlined for individuals with reduced kidney function. Healthcare professionals should exercise caution and consider the lack of data when prescribing to this patient population.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in relation to the use of this medication. Consequently, there is no information available regarding dosage adjustments, special monitoring requirements, or precautions for individuals with compromised liver function. It is recommended that healthcare providers exercise caution when prescribing this medication to patients with hepatic impairment, given the absence of data to guide treatment decisions in this population.

Overdosage

There is currently no specific information available regarding overdosage for this medication. Healthcare professionals are advised to monitor patients closely for any unusual symptoms or adverse effects that may arise. In the event of suspected overdosage, it is recommended to initiate supportive care and symptomatic treatment as necessary.

Healthcare providers should consider contacting a poison control center or a medical toxicologist for further guidance on management strategies tailored to the individual patient's needs. Continuous assessment and monitoring of vital signs and clinical status are essential in managing any potential complications associated with overdosage.

Nonclinical Toxicology

No teratogenic effects were reported in the studies conducted. Additionally, no adverse developmental outcomes were observed, indicating a lack of non-teratogenic effects.

There is no specific nonclinical toxicology data available for review. Furthermore, no animal pharmacology and toxicology data have been provided.

Postmarketing Experience

No postmarketing experience details are available in the provided data.

Patient Counseling

Healthcare providers should inform patients that if the material is not delivered to a customer classified as a non-federal (NF) entity, it is considered "Not Approved for Human Drug Use." It is essential for patients to understand the implications of this designation and the importance of ensuring that the material is handled appropriately. Providers should encourage patients to ask questions if they have any concerns regarding the use or approval status of the material.

Storage and Handling

The product is supplied in a well-ventilated area, ensuring that the container remains tightly closed to maintain integrity. It is essential to protect the product from physical damage during storage and handling. Appropriate safety equipment should be utilized when handling the product to ensure safety.

The product must not be exposed to heat or flame, as this could compromise its quality and safety. Disposal should be conducted in accordance with local regulations to ensure compliance with environmental and safety standards.

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 Messer LLC. 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 (NDA205766) 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.