fda
2 records
FDA Drug Recall: Atorvastatin Calcium Tablets USP 40 mg, 1000-count bottle, Rx Only, Manufactured
2025-04-09
Class II — Failed dissolution specifications: lower than specifications
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FDA Drug Recall: Posaconazole Delayed-Release Tablets, 100 mg, 60-count bottle, Rx Only, Manufact
2023-02-15
Class II — Failed Impurities/Degradation Specifications: High Out Of Specification degradation results.
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fda_adverse
4 records
FDA AE Manufacturer: Biocon Pharma Inc,
Drug adverse event reporter — Product: SIMVASTATIN
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FDA AE Manufacturer: Biocon Pharma Inc
Drug adverse event reporter — Product: ROSUVASTATIN CALCIUM
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FDA AE Manufacturer: Biocon Pharma Inc.
Drug adverse event reporter — Product: FAMOTIDINE
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FDA AE Manufacturer: BIOCON PHARMA INC.,
Drug adverse event reporter — Product: LENALIDOMIDE
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