Global pharma major Lupin Limited has announced that it has received approval from the United States Food and Drug Administration (U.S. FDA) for its Abbreviated New Drug Application (ANDA) for its ...

Dr Reddy's Laboratories received seven observations from the USFDA following an inspection of its Bollaram facility. The ...

Dr Reddy's Laboratories (DRL) informed that on Tuesday, 19 November 2024, US Food and Drug Administration (USFDA) completed its Good manufacturing practice (GMP) inspection at API manufacturing ...

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

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

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

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 ...

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

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, ...

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