Sun Pharma's Doxycycline Recall: FDA Cites CGMP Deviations, Highlighting Generic Drug Supply Risks
Sun Pharmaceutical Industries, Inc. faced a Class II recall of Doxycycline Capsules, USP, 75 mg, due to significant CGMP deviations at its manufacturing site. This voluntary action, impacting 624 bottles distributed nationwide, underscores critical quality control vulnerabilities. Procurement and regulatory teams must scrutinize supplier compliance, especially for generic tetracycline-class drugs, to mitigate supply chain disruptions and ensure product integrity.