The latest recall number for this product is D-0373-2023 and the recall is currently ongoing
, originally initiated on 10-22-2019 for the product Atorvastatin Calcium Tablets, USP 40 mg*, 1,000 count bottles, Rx Only, Manufactured by: Apotex Inc
According to the most recent FDA Enforcement Report, Apotex is voluntarily Apotex Corp
3 Recommended Dosage in Pediatric Patients 10 Years of Age and Older with HeFH
The company detected the carcinogen N-nitrosodimethylamine (NDMA) in the active ingredient for the blood pressure drug
Atorvastatin tablet, Apotex, 80 mg, 1000 count, NDC 60505-2671-08; Atorvastatin tablet, Sandoz, 40 mg, 90 count, NDC 00781-5384-92; Reason for the Shortage
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Reddy's Laboratories is pulling from distribution more than 236,000 bottles of its generic copy of cholesterol drug Lipitor, initiating four voluntary recalls in the U
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Issues Voluntary Nationwide Recall of Guanfacine Extended-Release Tablets 2mg due to trace amounts of Quetiapine Fumarate Media Contact: Jordan Berman, Vice President, Global Corporate Affairs Tel: 1 (416) 749-9026 Ext
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Although not all of these side effects may occur, if they do occur they may need medical attention
5 billion
NDC Number : 60505-2579-08
" Harrow Licenses Canadian Rights to Apotex for Five Branded Ophthalmic Pharmaceutical Products
, Canada's largest pharmaceutical company, today jointly announced an exclusive out-licensing agreement under which Apotex will market and distribute VERKAZIA® and over-the Atorvastatin is a statin medication used to prevent cardiovascular disease in those at high risk and to treat abnormal lipid levels
Apotex, based in Fort Lauderdale, Florida suburb of Weston, recalled adult anti-depressant Paroxetine in 10 mg, 20 mg, 30 mg, 40 mg Jordan Berman
More Recalls, Market Withdrawals, & Safety Alerts
33 lb
Atorvastatin Calcium 20mg Tablets, 90 coun t 16729-0045-15 R2100305 exp
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Grapefruit may interact with atorvastatin and cause side effects
The last Recall Enforcement Report for Atorvastatin Calcium with NDC 60505-2671 was initiated on 10-22-2019 as a Class III recall and it is currently completed
Learn more about its uses, dosage, side effects and interactions from this consumer medicine information page
26 lb
No matter where a medication is produced it cannot be brought into the usa without passing FDA standards
In an increasingly competitive market environment, Apotex continually strives to introduce quality, affordable medicines to consumers
Irbesartan and Irbesartan/hydrochlorothiazide (HCTZ) Tablets - Consumer-level Recall
60505-2531-06
Mylan said it was recalling the 4,005,177 bottles and 1,527 cartons because of the "potential of an elevated bioburden with identification of Several drugs containing valsartan being recalled due to contamination with a potential carcinogen (advisory July 9, 2018) Ranitidine recalls Ranitidine
recalled close to 6,400 bottles of atorvastatin calcium tablets due to a report of an embedded object in one tablet
Enter VIN here: Information about the prescription drugs manufactured by Apotex Corp
× APO A10 Pill - white oval, 9mm
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The affected products table has been updated with information on the recall
HYDERABAD: Dr Reddy's Laboratories has initiated voluntary recall of over 80,000 bottles of its drug Atorvastatin Calcium Tablets 10mg, 20mg and 40mg from the US market due to quality concerns
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, originally initiated on 10-22-2019 for the product Atorvastatin Calcium Tablets, USP 40
A California drug distributor is recalling hundreds of packages of a generic cholesterol drug after Canadian generics producer Apotex found the pills failed
Atorvastatin calcium tablets can cause serious muscle problems that can lead to kidney problems, including kidney
Atorvastatin tablet, Apotex, 80 mg, 1000 count, NDC 60505-2671-08; Atorvastatin tablet, Sandoz, 40 mg, 90 count, NDC 00781-5384-92; Reason for the
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The recalled product might cause a temporary health problem or slight threat of a serious nature
Description: Atorvastatin Calcium Tablets, USP 40 mg*, 1,000 count bottles, Rx Only, Manufactured by: Apotex Inc
Apotex's generic version was launched under the name of Apo-Atorvastatin
Patients who require reduction in LDL-C greater than 45% may be started at 40 mg once daily
” Recall classifications
Common side effects include joint pain, diarrhea, heartburn, nausea, and muscle pains
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Zero side effects
The recall was issued Nov
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It can help prevent heart attack, stroke and other cardiovascular problems
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40 mg*, 1,000 count bottles, Rx Only, Manufactured by: Apotex Inc
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Levoleucovorin 250mg/25 mL single-dose vial Consumer-Level