Glenmark Pharmaceuticals Inc., USA has been granted final approval by the United States Food & Drug Administration (USFDA) for Telmisartan and Hydrochlorothiazide Tablets USP, 40 mg/12.5 mg ...

According to an FDA notice, Torrent has recalled 36 lots of losartan potassium tablets USP and 68 lots of losartan potassium/hydrochlorothiazide ... valsartan, telmisartan and olmesartan medoxomil ...

Glenmark Pharmaceuticals Inc, USA has been granted final approval by the United States Food & Drug Administration (USFDA) for Telmisartan and Hydrochlorothiazide Tablets USP in the strengths of 40 ...

The bottle was supposed to contain hydrochlorothiazide tablets USP 12.5 milligrams, a medication used to treat high blood pressure. Instead, they contained a different kind of diuretic ...

Consumers that may have Telmisartan Tablets, USP, 20 mg which is being recalled should not discontinue use until speaking with their pharmacist or healthcare professional for a replacement before ...

Irbesartan and Hydrochlorothiazide tablet USP, 150mg/12.5mg and 300mg/12.5mg were also packaged in 30- and 90-count bottles and distributed to wholesalers, drug chains, mail-order pharmacies and ...

It's recalling: All batches of irbesartan tablets USP 75mg, 150mg and 300mg All batches of irbesartan and hydrochlorothiazide tablets USP, 150mg/12.5mg and 300mg/12.5mg Lupin says it received four ...

The recall concerns lot Nos. QE2021005-A and QE2021010-A of Quinapril and Hydrochlorothiazide Tablets USP 20mg / 12.5mg in 90-count bottles from Aurobindo Pharma with an expiration date of January ...