Major Indian pharmaceutical companies are recalling products in the US due to problems with their manufacturing processes.

Indian pharmaceutical companies Dr Reddy's Laboratories, Sun Pharma, and Aurobindo Pharma are recalling their products in the US due to manufacturing problems.

May 19th 2024.

Major Indian pharmaceutical companies are recalling products in the US due to problems with their manufacturing processes.
In recent news, several pharmaceutical companies in India have issued recalls for their products in the US due to concerns over manufacturing issues. Among the companies involved are Dr Reddy's Laboratories, Sun Pharma, Aurobindo Pharma, as well as others.

According to reports from the US Food and Drug Administration, Dr Reddy's Laboratories has recalled their product Javygtor Powder for Oral Solution due to it being deemed a "Sub-potent Drug." This particular product is used to treat a condition known as hyperphenylalaninemia, which is characterized by high levels of phenylalanine in the blood. In addition to this, the company has also issued a recall for another lot of the same product for the same reason. These recalls, classified as Class I by the FDA, began on April 8.

Similarly, Sun Pharma has also issued a recall for one of their products, Amphotericin B Liposome for Injection, which is used to treat fungal infections. This recall, classified as Class II, began on April 19 due to concerns that the product was "Out of specification for assay." This means that the product may not be as effective as it should be in treating the intended condition.

Aurobindo Pharma has also joined in on the recalls, with 13,605 bottles of their product Clorazepate Dipotassium Tablets being pulled from the US market. These tablets are used to treat anxiety, and the recall was initiated on April 24 due to concerns of "Discoloration: Dotted and yellow spots on tablets." This could potentially affect the effectiveness and safety of the product.

Furthermore, the USFDA has also reported that FDC Ltd is recalling over 380,000 units of their product Timolol Maleate Ophthalmic Solution, which is used to treat glaucoma. The company has issued this recall due to a "Defective Container," which could potentially compromise the integrity of the product.

It should also be noted that earlier this month, other drug makers such as Cipla and Glenmark have also issued recalls for their products in the US market, citing similar concerns over manufacturing issues. This serves as a reminder of the importance of adhering to strict quality control measures in the pharmaceutical industry.

In conclusion, it is clear that these recalls highlight the need for pharmaceutical companies to prioritize the safety and effectiveness of their products. As consumers, it is important to stay informed and cautious when it comes to medications and to always consult a healthcare professional if there are any concerns.

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