fda
4 records
FDA Drug Recall: Discount Drug Mart, Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg /
2020-03-11
Class III — Labeling: Incorrect or Missing Lot and/or Expiration date.
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FDA Drug Recall: Ranitidine 150 mg tablets, 24 count bottles, NDC 37808-196-01.
2020-01-15
Class II — CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API
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FDA Drug Recall: Ranitidine 150 mg tablets, 130 count bottles, NDC 37808-196-04.
2020-01-15
Class II — CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API
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FDA Drug Recall: Smart Sense Regular Strength Aspirin Tablets, 325 mg packed in a) 100 count UPC
2019-08-14
Class III — Labeling; Incorrect or Missing Lot Number and/or Exp Date; Product has an incorrect expiration date of 9/2022 applied to the labeling, where the actual expiration date is 10/2021.
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fda_adverse
1 records
FDA AE Manufacturer: AAA Pharmaceutical, Inc.
Drug adverse event reporter — Product: IBUPROFEN
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