Sun Pharma, Dr Reddy’s, Aurobindo, Jubilant recall products in US Press Trust of India Mar 14, 2021 The Indian firms have initiated recall of these products for various reasons including failed impurities/degradation…
Lupin, Aurobindo recall drugs in US market Press Trust of India Feb 15, 2021 Lupin Pharma is recalling 46,479 bottles of Oseltamivir Phosphate for Oral Suspension while AuroMedics Pharma, a unit of Aurobindo…
Cipla, Strides Pharma recall drugs in the US market Press Trust of India Jan 10, 2021 Cipla has recalled packets of esomeprazole magnesium for delayed-release oral suspension while Strides Pharma has recalled…
DCGI asks state drug controllers to recall ulipristal acetate tablets from market Usha Sharma Nov 19, 2020 The decision is based on the PRAC recommendations and reported cases of liver injury in the EU
Sun Pharma, Strides Pharma recall drugs in the US Press Trust of India Oct 11, 2020 Sun Pharma is recalling 747 bottles of generic diabetes drug due to higher levels of NDMA while Strides Pharma is recalling 11,280…
Marksans Pharma expands recalls of metformin hydrochloride tablets EP News Bureau Oct 4, 2020 It is due to NDMA content in some lots that exceed the acceptable daily intake limit of 96ng/day
Lupin recalls around 5.61 lakh pouches of Mibelas 24 Fe in the US Press Trust of India Aug 21, 2020 The product, manufactured in India and then supplied in the US market by Lupin Pharmaceuticals, is used to prevent pregnancy
Lupin, Sun Pharma recall drugs in US market Press Trust of India Aug 9, 2020 Lupin is recalling 11,688 bottles of Lisinopril tablets USP, 10 mg while Sun Pharma is recalling 3,516 bottles of Clonazepam…
Lupin recalls 35,928 bottles of Cefdinir, generic antibiotic drug in the US Press Trust of India Aug 2, 2020 The medication is used to treat pneumonia, otitis media, strep throat, and cellulitis
Lupin, Granules India recall around 9.71 lakh bottles of diabetes drug in the US Press Trust of India Jul 26, 2020 Various companies across the globe have announced similar recalls for the product after the USFDA pointed out the presence of NDMA…