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FAILED DISSOLUTION SPECIFICATIONS
Glenmark recalls 6,528 bottles of blood pressure drug in USAs per the USFDA, a Class II recall is initiated in a situation in which the use of, or exposure to, a violative product may cause temporar...14 Apr, 2024, 03.11 PM IST- Sun Pharma, Lupin recall drugs in US market: USFDASun Pharmaceutical is recalling the affected lot that was produced at the drugmaker's Dadra-based facility. The company is recalling the lo...17 Dec, 2023, 10.48 AM IST
- Zydus unit recalls 7,248 bottles of Oxybutynin Chloride tablets in USNew Jersey-based Zydus Pharmaceuticals (USA) Inc. is recalling the affected lot due to "Failed Dissolution Specifications", the USFDA state...13 Oct, 2023, 04.07 PM IST
- Sun Pharma recalls over 34k bottles of generic drug in US due to manufacturing issuesPrinceton (New Jersey) based Sun Pharmaceutical Inc is recalling the affected lot due to "Failed Impurity (Deacetyl Diltiazem Hydrochloride...11 Feb, 2023, 01.40 PM IST
- Manufacturing issues led drug makers Glenmark, Sun Pharma, Dr Reddy's to recall products in USAs per the US health regulator, a class II recall is initiated in a situation in which use of, or exposure to, a violative product may caus...14 Aug, 2022, 01.09 PM IST
- Cipla recalls 4,800 bottles of anti-HIV tablets from USAs per the latest Enforcement Report by the United States Food and Drug Administration (USFDA), the reason for the recall of the bottles is...30 Dec, 2018, 01.07 PM IST
- Lupin recalls 12,480 bottles of anti-depressant drug from USLupin Pharmaceuticals Inc is recalling 12,480 bottles of Paroxetine extended-release tablets in the strength of 12.5 mg manufactured by Lup...19 Jul, 2017, 03.54 PM IST
- Dr Reddy's recalls 3.25 lakh cartons Cipla-made acne drug from USThe ongoing voluntary class II recall is nationwide in the USA and Puerto Rico, the United States Food and Drug Administration (USFDA) said.14 Jun, 2017, 03.18 PM IST
- Aurobindo Pharma, Cadila recall drugs from US marketPantoprazole Sodium delayed-release tablets are used for treatment of erosive inflammation of the esophagus due to acid reflux.21 Sep, 2016, 05.57 PM IST
- 2,839 bottles of Sun Pharma Inc being recalled in USThe ongoing nationwide voluntary recall by Nostrum Laboratories Inc for Nitrofurantoin Oral Suspension, USP, 25 mg/5 mL is a class II recal...22 Jun, 2016, 02.55 PM IST
- Apotex Inc recalls hypertension drug made by Indian armApotex Inc has initiated a recall of 2,075 bottles of blood pressure treatment tablet 'Verapamil Hydrochloride' manufactured by Bangalore b...13 Oct, 2015, 09.27 PM IST
- Sun Pharma, Wockhardt recall drugs from US marketSun Pharma initiated voluntary recall of Bupropion Hydrochloride Extended-¬release Tablets USP (SR), while Wockhardt started recalling its ...30 Aug, 2015, 12.38 PM IST
- Dr Reddy's Laboratories recalls anti-seizure, hypertension drugs from US marketThe firm has started recalling Divalproex Sodium extended-release tablets as it has failed dissolution tests.29 Jun, 2015, 01.02 PM IST
- Sun Pharma recalls 5,322 bottles of Ketorolac eye drop in USLast month, the drug major had recalled 3,263 bottles of epilepsy drug in US market for failing "dissolution specifications".08 Mar, 2015, 11.48 AM IST
- Sun Pharma recalls 3,263 bottles of epilepsy drug in USAs per the information available, Sun Pharma Global Fze, a US-based unit of the company, is recalling the drug for failing "dissolution spe...23 Feb, 2015, 07.00 PM IST
- Sun Pharmaceutical Industries recalls Venlafaxine Hydrochloride after failing a dissolution testThe recall was made by Sun Pharma’s US subsidiary Caraco Pharmaceutical Laboratories for drugs manufactured in the company’s Indian facilit...12 Jul, 2014, 02.21 AM IST
- Dr Reddy's recalls over 13,000 bottles of hypertension drug: FDADr Reddy's Laboratories Ltd is recalling 13,560 bottles of the high blood pressure drug metoprolol succinate in US after it failed a dissol...19 Jun, 2014, 12.27 PM IST
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