Cipla gets USFDA approval for HIV drug

Pharmaceutical firm Cipla has got tentative approval from the USFDA for its abbreviated new drug application (ANDA) for anti-HIV/AIDS drug Slamivudine.

NEW DELHI: Pharmaceutical firm Cipla has got tentative approval from the USFDA for its abbreviated new drug application (ANDA) for anti-HIV/AIDS drug Slamivudine.
According to information available on the USFDA website, the tentative approval is for the oral solution of strength 10mg per ml.
The drug is in a class of medications called nucleoside reverse transcriptase inhibitors. It works by stopping the spread of the HIV and hepatitis B viruses.
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Business News › Industry › Healthcare/Biotech › Pharmaceuticals › Cipla gets USFDA approval for HIV drug
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