List of Drugs A-Z tool - Find drug information on prescription drugs, medicines & supplements including side effects, drug interactions & generic drug name.

Class I recalled products have the potential to cause serious harm or death. FDA will determine official alternatives by using the criteria established through notice-and-comment rulemaking, as it has done with albuterol.Information regarding FDA's approval of these inhalers is available here.

In six categories of drugs, both brand-name and generic versions were tested.

A recall is a voluntary action taken by a company to remove a defective drug product from the market. Each drug name in the list below is linked to the drug’s regulatory history, including label, from Drugs@FDA. What is an active moiety?

Manufacturer GlaxoSmithKline has issued a voluntary recall for Ventolin HFA, a rescue inhaler used for bronchospasm (asthma).. Drug recalls may be conducted on a company’s own initiative or by FDA request. As FDA approves new non-CFC inhalers, we will add that information to this page.Drugs are listed in alphabetical order by active moiety, with specific brands available listed under each active moiety. Many different drug products may be marketed with the same active moiety.Each drug name in the list below is linked to the drug’s regulatory history, including label, from Drugs@FDA. The drugs that tested included six asthma drugs, four for treating epilepsy, four high blood pressure drugs, four drugs for treating heart arrhythmias, a birth control pill, one antibiotic, a drug for treating depression, and a so-called blood-thinning drug.

Of those recalls, the FDA classified 139 as Class I.

* Drugs@FDA includes information about drugs, including biological products, approved for human use in the United States (see FAQ), but does not include information about FDA-approved products regulated by the Center for Biologics Evaluation and Research (for example, vaccines, allergenic products, blood and blood products, plasma derivatives, cellular and gene therapy products). The Recalls, Market Withdrawals & Safety Alerts are available on FDA’s website for three years before being archived. If you have a medicine that has been recalled, talk to your health care professional about the best course of action for your health, including the possibility of returning the product to the store in which you purchased it.Stores generally have a return and refund policy when a company has announced a recall of its products. An active moiety is the part of a drug that makes the drug work the way it does. VENTOLIN HFA (albuterol sulfate) aerosol, metered. Generally, Class I recall notifications provide instructions with actions for patients. Between November 2018 and April 2019, close to 300 lots of drugs containing losartan were recalled because potentially cancer-causing substances were found in … These products aren't necessarily "official" direct alternatives to CFC Metered Dose Inhalers, but may in many patients serve as a useful medication that could replace the need for a particular CFC Metered Dose Inhaler. An official website of the United States government This is a class II recall, the most common type of recall, which means that there is a situation where the use of the recalled medication may cause temporary or medically reversible adverse health consequences, but the likelihood of serious adverse effects is small. If you are taking the popular blood pressure drug, losartan, you may have seen the news reports about contamination. Information by Drug Class

This is a list of the worst drug recalls since the FDA became responsible for approving drugs in 1962. FDA recommends that patients follow the instructions provided by the recalling company. NDC Code(s): 35356-166-01, 35356-166-02, 35356-166-08 An official website of the United States government: Many inhalers that do not use chlorofluorocarbons (CFC) are already available for the treatment of asthma and chronic obstructive pulmonary disease.

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