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Weve seen that previously in a warning letter to Annovex Pharma: Your facility failed to submit a report to FDA in June 2024 identifying the drug products that you compounded during the previous 6-month period, including Heparin 4 units/mL in 0.9% Sodium Chloride (b)(4) IV bag, Phenylephrine 100 mcg/ml in 0.9% Sodium Chloride Solution 10ml syringe, and Phenylephrine HCl 25 mg in 0.9% Sodium Chloride 250 mL Bag

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Nephrology 29 , 457469 (2024)

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