"This is to inform you that the United States Food & Drug Administration (USFDA) today completed a GMP inspection at our API ...

Dr Reddy's Laboratories and FDC Ltd issued voluntary recalls for medications in the US market due to manufacturing defects.

The FDA would provide manufacturers with appropriate time to either reformulate drugs containing oral phenylephrine or remove ...

Dr Reddy's Laboratories and FDC Ltd, are recalling generic medications in the US over manufacturing defects. According to the ...

A team of Canadian researchers has found an existing US Food and Drug Administration-approved drug that could significantly ...

As per the USFDA, Princeton-based Dr Reddy's Laboratories Inc is recalling 2,040 bottles of 15 mg Morphine Sulfate ...

Global pharma major Lupin Limited on Friday announced that it has received tentative approval from the United States Food and ...

The US Food and Drugs Administration (USFDA) conducted an inspection at the company's manufacturing facility in Virgonagar, ...

Alembic Pharmaceuticals stated that it gained final FDA approval for the Diltiazem Hydrochloride Extended-Release capsules, ...

Six types of brie cheese sold at Aldi stores in New Jersey and 11 other states have been recalled due to possible listeria ...

The inspection, which took place in September, determined that the facility is in compliance with all applicable USFDA ...

These capsules will be available in dosages of 120 mg, 180 mg, 240 mg, 300 mg, and 360 mg, offering a generic alternative to ...