lamotrigine recall 2020 prandin

The NDC number of the drug is 51672-4131-1.The recalled Lamotrigine was distributed to wholesale distributors in the U.S. from Aug. 23 to Aug. 30, 2019. A physician or healthcare provider should be contacted if a consumer has any problems related to the affected medication.Questions about the recall can be directed to Taro at 1-866-923-4914, Monday through Friday from 7 a.m. to 7 p.m. CST or by email at Shares of Taro Pharmaceuticals stock were down 0.28% as of 9:43 a.m. EST on Monday.

Enalapril Maleate is a drug substance indicated for hypertension and congestive heart failure. MedWatch Safety Alerts are distributed by the FDA and published by Drugs.com. Psychiatry > General Psychiatry Lamotrigine Recall; Minimum Wage and Suicide Risk — News and commentary from the psychiatry world. The NDC and lot number associated with Taro’s recalled product is as follows: Lamotrigine 100 mg tablets (NDC 51672-4131-01; Lot 331771; expiration date June 2021). For questions or concerns, please reach out to Envolve Pharmacy Solutions’ Pharmacy Department by calling 1-800-782-2221.You will need Adobe Reader to open PDFs on this site.You will need Adobe Reader to open PDFs on this site.Washington Apple Health and Apple Health Foster Care plans issued by Coordinated Care of Washington, Inc.Ambetter plan issued by Coordinated Care Corporation Taro has not received any reports of adverse reactions from the recalled medication to date.Consumers that have been prescribed the Lamotrigine tablets should stop using the medication and return it to their pharmacy. On January 10, 2020, the U.S. Food and Drug Administration (FDA) announced that Taro Pharmaceuticals U.S.A., Inc. was recalling one lot of Lamotrigine Tablets to the consumer level due to cross-contamination with Enalapril Maleate.

Date: The recall affects 100 mg Lamotrigine USP tablets sold in 100-count white plastic bottles with a screw-cap closure. Following is a list of possible medication recalls… Prandin FDA Alerts. This single lot of Lamotrigine 100 mg Tablets Lot #331771 (expiration date June 2021) was found to have been cross-contaminated with a small amount of … The company is recalling one lot of Lamotrigine tablets of 100 mg strength that are packaged in and 100 count white plastic bottles with expiration … Taro Pharmaceuticals Recalls Lamotrigine 100 mg Tablets Due to Cross Contamination Taro Pharmaceuticals has issued a voluntary recall of 1 lot of Lamotrigine 100 mg tablets, lot # 331771 (expiring June 2021) in 100 count bottles. This lot of Lamotrigine was found to have been cross contaminated with a small amount of Enalapril Maleate.

On January 10, 2020, the U.S. Food and Drug Administration (FDA) announced that Taro Pharmaceuticals U.S.A., Inc. was recalling one lot of Lamotrigine Tablets to the consumer level due to cross-contamination with Enalapril Maleate.Taro Pharmaceuticals U.S.A., Inc. is voluntary recalling one lot of Lamotrigine 100 mg tablets to the consumer level due to cross-contamination with a small amount of another drug substance (Enalapril Maleate) used to manufacture another product at the same facility.
Lamotrigine 100 mg tablets are indicated for Epilepsy and Bipolar disorder. Enalapril Maleate is also associated with risk of birth defects in a developing fetus. Taro Pharmaceuticals announced the voluntary recall of 1 lot of lamotrigine 100mg tablets to the consumer level due to cross-contamination with a small amount of enalapril maleate. There is potential with chronic exposure to Enalapril Maleate to impact users particularly if they are small children or pregnant women. January 10, 2020 -- Taro Pharmaceuticals U.S.A., Inc. (“Taro” or the “Company”) is voluntarily recalling one (1) lot of Lamotrigine 100 mg Tablets, Lot # 331771 (expiration date June 2021) in 100 count bottles, NDC 51672-4131-1 to the consumer level. The FDA Alert(s) below may be specifically about Prandin or relate to a group or class of drugs which include Prandin (repaglinide). Use of the recalled Lamotrigine 100 mg tablets could potentially result in exposure to a small amount of Enalapril Maleate, if present in the product in question. Therefore, there is risk associated with the continued, long-term use of the recalled Lamotrigine 100 mg tablets.Please immediately check your medical supplies, quarantine any drug products impacted, and do not administer them.

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