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The Financial Express · 1d

USFDA proposes removal of common decongestant from shelves after finding it ineffective

The FDA would provide manufacturers with appropriate time to either reformulate drugs containing oral phenylephrine or remove such drugs from the market, it stated.

Ars Technica · 2d

After decades, FDA finally moves to pull ineffective decongestant off shelves

Specifically, the FDA issued a proposed order to remove oral phenylephrine from the list of drugs that drugmakers can include in over-the-counter products—also known as the OTC monograph. Once removed,

FDA proposes pulling ineffective cold medicine from shelves

When you're feeling under the weather, you likely grab your go-to cough and cold medicine. But are all the ingredients helping you fight off that cold?

The Financial Express1d

USFDA grants tentative approval to Lupin’s generic formulation to treat HIV infection

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

Grand Junction-Montrose KKCO on MSN8d

USFDA says specific type of onions used in McDonald’s hamburgers likely linked to E. coli outbreak

Fresh-slivered onions used on McDonald’s Quarter Pounder hamburgers appear to be the likely source of a recent E. coli ...

Hosted on MSN6d

Dr Reddy's recalls over 3.3 lakh bottles of generic medication in US: USFDA

Besides, the drug maker is recalling 35,880 and 10,584 bottles of 60 mg and 90 mg strengths, respectively, USFDA said. The ...

Cipla shares jump 10% after USFDA paves the way for an important drug launch

Cipla Ltd. shares jumped over 10% in early trading on Thursday after the USFDA classified its Goa facility as a "Voluntary ...

Johnson & Johnson MedTech bags USFDA nod for the Varipulse Pulsed Field Ablation Platform for atrial fibrillation

Irvine: Johnson & Johnson MedTech has announced the U.S. Food & Drug Administration (FDA) approval of the VARIPULSE Platform ...

2d

Andhra Sugars’ aspirin facility gets USFDA nod

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

Granules India rises 3% after USFDA inspection at Andhra Pradesh plant shows no issues

Opening higher at ₹575.95 apiece on the BSE, shares of Granules India Ltd. rose further to touch an intraday high of ₹590.

If you bought soft cheese from this NJ store: toss it

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

10d

Indoco Remedies gets USFDA nod for smoking cessation drug; stock rises

Indoco Remedies receives USFDA approval for Varenicline Tablets, plans to manufacture at Goa facility, showcasing growth in ...

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