Generic Synthroid manufacturers adhere to stringent FDA guidelines. The process begins with sourcing high-quality levothyroxine sodium. Manufacturers use precise synthesis methods, ensuring consistent potency and purity. Rigorous testing occurs at every stage, including raw material analysis and intermediate product assessments.
Quality Assurance Measures
Quality control involves sophisticated analytical techniques like High-Performance Liquid Chromatography (HPLC) to verify the levothyroxine content. Dissolution testing confirms the drug’s ability to dissolve and release medication effectively. Stability studies under various conditions guarantee product longevity. Finally, the finished product undergoes multiple inspections to confirm compliance with all quality standards before distribution.
Batch Release Criteria
Each batch of generic Synthroid must meet precise specifications for active ingredient content, purity, and dissolution. Only batches passing all quality control tests receive release for market distribution. This multi-layered approach assures consumers receive a product equivalent to the brand-name alternative.
