Torrent Pharmaceuticals Limited is expanding its recall for Losartan Potassium Tablets USP and Losartan Potassium/hydrochlorothiazide tablets, USP, to the
Losartan and Hydrochlorothiazide oral tablet, Rising Pharmaceuticals, 100 mg/ 12
Update [5/6/2019] FDA is alerting patients and health care professionals to a voluntary recall of 19 lots of losartan potassium tablets made by Vivimed Life
RECALLING FIRM: Strides Pharma
National Drug Code Directory
The product's dosage form is tablet, film coated and is administered via oral form
The product is distributed in 2 packages with assigned NDC codes 68180-216-06 30
The last Recall Enforcement Report for Losartan Potassium 25 Mg with NDC 64380-933 was initiated on 06-26-2023 as a Class II recall due to presence of foreign substance: presence of a small piece of blue plastic embedded in the tablet
05-18-2022
, 101, 102, 107 & 108, SIDCO Pharmaceutical Complex, Alathur, Kanchipuram - 603 110, Tamilnadu, India, Distributed by: Strides Pharma Inc
The NDC Packaged Code 62332-050-90 is assigned to a package of 90 tablet, film coated in 1 bottle of Losartan Potassium And Hydrochlorothiazide, a human prescription drug labeled by Alembic Pharmaceuticals Inc
Date Brand Name(s) Product Description Recall Reason Description Company Name Terminated Recall Excerpt; 11/15/2023: Dr
The product's dosage form is tablet, film coated and is administered via oral form
The product's dosage form is tablet, film coated and is administered via oral form
National Drug Code (NDC) Lot Number Expiration Date; Losartan, 50mg: 13668-409
The generic name of Losartan Potassium is losartan potassium
The NDC code 62332-050 is assigned by the FDA to the product Losartan Potassium And Hydrochlorothiazide which is a human prescription drug product labeled by Alembic Pharmaceuticals Inc
This product What is NDC 72865-141-90? The NDC Packaged Code 72865-141-90 is assigned to a package of 90 tablet, film coated in 1 bottle of Losartan Potassium, a human prescription drug labeled by Xlcare Pharmaceuticals, Inc