Last Updated on March 22, 2025 by The Health Master
USFDA approval
The United States Food and Drug Administration approval (USFDA approval) has been granted to Zydus Lifesciences to manufacture and distribute Methenamine Hippurate Tablets USP, 1 gram.
The USFDA approval for the said drug is a generic version of Hiprex Tablets, 1 gram, offering a more accessible option for patients suffering recurrent urinary tract infections (UTIs).
Chronic UTI Management:
Methenamine Hippurate tablets play an important role in the treatment and therapy of frequently recurring UTIs.
This is particularly important for patients requiring long-term management to prevent persistent infections.
Indication:
- Long-term UTI prevention.
- Individuals with recurring UTIs.
- Reduces the burden of chronic infections.
Manufacturing:
The manufacturing of these tablets will be done at the manufacturing facility of Zydus Lifesciences Ltd (SEZ) situated in Ahmedabad, Gujarat, India.
Q: What is the use of Methenamine Hippurate?
A: Methenamine Hippurate is used for the prevention and suppression of frequently recurring urinary tract infections (UTIs).
Q: Where will the Methenamine Hippurate tablets be manufactured?
A: These tablets will be manufactured at the manufacturing facility of Zydus Lifesciences Ltd (SEZ), situated in Ahmedabad, Gujarat, India.
Q: What is an ANDA?
A: It is known as the Abbreviated New Drug Application (ANDA), which is filed with the USFDA for approval to market a generic drug that is bioequivalent to a brand-name drug.
Disclaimer: This article contains information obtained from the source mentioned below. Our team made changes in the format to rewrite and present the news or article in a unique format.
Disclaimer: The information we have provided is for general knowledge and for informational purpose only and it cannot be treated as medical advice. Always consult your doctor for any health issues and / or for the treatment of the same. The Health Master does not claim responsibility for this information.
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