Potency verification testing of Furosemide 80mg tablets was conducted to ensure rapid and potent diuretic effect. The analysis included chlorination stability and degradation product assessment.
HPLC, GC-MS
| Parameter | Value |
|---|---|
| Sample Identification | FUROSEMIDA 80MG (Lote# FUR80-2024) |
| Concentration | 2.15 mg/mL ± 0.14 |
| Purity | 98.4% |
| Impurities | < 1.6% |
GC-MS analysis confirmed the anthranilic acid structure and detected no dechlorination products. HPLC testing demonstrated excellent stability with minimal furfural formation. The product shows consistent dissolution characteristics, ensuring rapid onset of diuresis crucial for acute fluid overload management.
The product exceeds quality standards for loop diuretic medications and demonstrates superior chemical stability.