Drug major Sun Pharmaceutical Industries is recalling over 1.10 lakh bottles of a generic medication used to treat erectile ...
J B Chemicals and Pharmaceuticals Ltd <JBCH.NS>::U.S. FDA APPROVED CO'S ABBREVIATED NEW DRUG APPLICATION FOR LORATADINE TABLETS USP 10 MG. J B Chemicals And Pharmaceuticals Sept-Qtr Consol Net PAT ...
All solid dosage forms and combination products with pseudoephedrine (loratadine 5 mg-pseudoephedrine 120 mg, loratadine 10 mg-pseudoephedrine ... hour extended-release tablets, and loratadine ...
There are no studies to date that have assessed the safety or efficacy of nonsedating antihistamines (e.g., loratadine ... 10 mg of pyridoxine and 10 mg of doxylamine combined in a single tablet ...
In April the Food and Drug Administration approved Grastek for grass pollen allergies in people age 5 through 65; Oralair for the treatment of certain pollen allergies in people 10 through 65 ...
The US arm of the domestic pharma major is recalling Tadalafil tablets in the American market, according to the latest ...
The company is recalling 73,957 bottles of 5 mg strength and 36,786 bottles of 20 mg strength, the US health regulator stated ...
Gold prices are trading down by 0.1% at ₹48,810 per 10 ... tablets in the American market. The Mumbai-based drug major is recalling the product in 30-count bottles of 5mg and 20 mg strengths.
Drug major Sun Pharmaceutical Industries is recalling over 1.10 lakh bottles of a generic ... recall of 22,752 blister packs of Loratadine-D extended-release tablets, used for the treatment ...
The Mumbai-based drugmaker is recalling the product in 30-count bottles of 5mg and 20 mg strengths ... of 22,752 blister packs of Loratadine-D extended-release tablets, used for the treatment ...