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Is Nizatidine the Same as Zantac? Clarifying the Difference After Recalls

3 min read

The active ingredient in Zantac, ranitidine, was entirely withdrawn from the market by the FDA in April 2020 due to potential contamination with the carcinogen NDMA. This has led many to question, 'Is nizatidine the same as zantac?'

Quick Summary

Nizatidine (Axid) and ranitidine (Zantac) are both H2 blockers but are not the same drug. The FDA requested a full market withdrawal of all ranitidine products due to NDMA contamination, while some nizatidine products were also recalled.

Key Points

  • Different Medications: Nizatidine (Axid) and ranitidine (Zantac) are distinct H2-blocker drugs, not the same compound.

  • Zantac is Recalled: All ranitidine (Zantac) products were completely withdrawn from the U.S. market in 2020 due to potential contamination with the carcinogen NDMA.

  • Nizatidine is Still Available: While some nizatidine (Axid) products were recalled, the medication was not fully withdrawn and remains available by prescription.

  • NDMA Impurity: NDMA is a probable human carcinogen that was found in ranitidine and some nizatidine products, with levels increasing over time in ranitidine.

  • Safe Alternatives Exist: Other H2-blockers like famotidine (Pepcid) and proton pump inhibitors (PPIs) like omeprazole (Prilosec) are safe alternatives for acid control.

  • Consult a Professional: Anyone concerned about acid reflux or previous use of ranitidine should consult a healthcare provider for the best treatment plan.

In This Article

Nizatidine and Zantac: Two Distinct H2 Blockers

No, nizatidine is not the same as Zantac. They are two different medications in the class of drugs called histamine-2 (H2) blockers, which reduce stomach acid. This makes them useful for conditions like heartburn and ulcers. The confusion often stems from their shared use and the fact that both were reviewed by the FDA for N-nitrosodimethylamine (NDMA) contamination.

The Zantac (Ranitidine) Recall

In April 2020, the FDA requested that all prescription and over-the-counter ranitidine products, including Zantac, be removed from the market. This was because lab tests found unacceptable levels of NDMA, a probable human carcinogen, in some ranitidine samples. NDMA levels increased over time, especially in warmer conditions. Consequently, Zantac and its generic are no longer sold in the U.S..

The Nizatidine (Axid) Situation

Nizatidine (Axid) was also evaluated by the FDA, and some products were recalled due to NDMA. Unlike ranitidine, however, the recall affected specific lots and formulations, and the drug was not completely removed from the market. Nizatidine, available by prescription, is still an option for treating acid-related issues. The NDMA levels found in some nizatidine products were generally lower than those in ranitidine.

Nizatidine vs. Zantac: A Comparison Table

The table below outlines the key differences between nizatidine and the now-recalled ranitidine.

Feature Nizatidine (Axid) Ranitidine (Zantac)
Drug Class H2-receptor antagonist H2-receptor antagonist
Brand Name Axid, Axid AR Zantac (before reformulation)
Status in US Remains on the market (prescription only) Withdrawn from market due to NDMA contamination
Active Ingredient Nizatidine Ranitidine
NDMA Contamination Some products recalled; contamination levels reportedly lower All products withdrawn due to unacceptable levels of NDMA
Formulations Capsule, oral solution Tablet, injection, effervescent tablet, syrup (before recall)
Common Side Effects Headache, dizziness, diarrhea, constipation Headaches, diarrhea, constipation (before recall)

Finding Safe Alternatives for Acid Suppression

Several medications are available as alternatives to ranitidine and have been tested by the FDA for NDMA.

  • Other H2-Blockers: Famotidine (Pepcid) and cimetidine (Tagamet) are H2-blockers without NDMA contamination issues and work similarly to reduce stomach acid.
  • Proton Pump Inhibitors (PPIs): PPIs like omeprazole (Prilosec), esomeprazole (Nexium), and lansoprazole (Prevacid) are stronger acid suppressants that block the final stage of acid production.
  • Antacids: Over-the-counter antacids provide quick, temporary relief by neutralizing stomach acid.

The Importance of Consulting a Healthcare Professional

It is essential to talk to a healthcare provider if you have acid-related symptoms or previously used ranitidine. They can recommend a safe and appropriate treatment plan and discuss potential risks related to NDMA exposure, although low levels of nitrosamines are generally not considered harmful by the FDA.

Conclusion: Separating the Facts from the Confusion

In summary, nizatidine and Zantac are not the same. Zantac, containing ranitidine, was completely removed from the U.S. market by the FDA due to excessive NDMA. While some nizatidine products were also recalled for similar reasons, the drug itself remains available by prescription. The ranitidine recall has led to increased use of other safe alternatives. Patients should consult a healthcare provider for treatment advice. The FDA's information indicates that NDMA levels in ranitidine can rise over time, posing a health risk.

The Fallout from the Ranitidine Recall

The recall of ranitidine raised concerns among users about health risks, particularly from long-term use. This event highlighted the importance of continuous drug safety monitoring and rigorous testing. It also drew attention to the potential instability of certain chemical compounds in medications and the possibility of carcinogenic impurities forming over time, especially with exposure to higher temperatures. While nizatidine is still a valid option, the ranitidine recall has significantly changed the H2-blocker market, increasing focus on alternative treatments and public awareness of drug safety.

Frequently Asked Questions

No, Zantac and all other ranitidine products were fully withdrawn from the U.S. market by the FDA in April 2020 and are no longer available for purchase.

Zantac was recalled because it was found to contain unacceptable levels of N-nitrosodimethylamine (NDMA), a probable human carcinogen. Lab testing showed that NDMA levels in ranitidine products increased over time and when stored at high temperatures.

Nizatidine was also investigated for NDMA contamination, leading to some product recalls, but it was not fully withdrawn like ranitidine. It remains available by prescription, and the FDA has not found widespread issues with other acid reducers.

While both are H2-receptor antagonists that reduce stomach acid, they are different chemical compounds. The primary distinction now is that ranitidine was permanently recalled due to NDMA, while nizatidine remains on the market.

Yes, Axid is a brand name for the generic drug nizatidine. You may find it sold as Axid-AR (formerly over-the-counter) or as generic nizatidine.

Alternatives include other H2-blockers like famotidine (Pepcid) and cimetidine (Tagamet), as well as proton pump inhibitors (PPIs) such as omeprazole (Prilosec), esomeprazole (Nexium), and lansoprazole (Prevacid).

N-nitrosodimethylamine (NDMA) is an environmental contaminant classified as a probable human carcinogen. Its presence in ranitidine products at increasing levels over time led to the market withdrawal due to potential cancer risk.

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.