Pharmaceutical Grade Fusidic Acid CAS 6990 -06-3
China Pharmaceutical Grade Fusidic Acid CAS 6990-06-3, Find details about China Fusidate Sodium, Fusidic Acid from Pharmaceutical Grade Fusidic Acid CAS 6990-06-3
| Product Name | Best quality Fusidic acid CAS 6990-6-3 |
| Appearance | white powder |
| Assay | 99.5% |
| Certificate | ISO 9001 |
| Test | HPLC |
| Packing | Bag, drum |
| MF | fos |
| StorageTemperature | Keep in a cool, dry, dark location in a tightly sealed container or cylinder |
Fusidic acid is a bacteriostatic antibiotic that is often used topically in creams and eyedrops, but may also be given systemically as tablets or injections. The global problem of advancing antimicrobial resistance has led to a renewed interest in its use recently,
Fusidic acid is active in vitro against Staphylococcus aureus, most coagulase-negative staphylococci, Beta-hemolytic streptococci, Corynebacterium species, and most clostridium species. Fusidic acid has no known useful activity against enterococci or most Gram-negative bacteria (except Neisseria, Moraxella, Legionella pneumophila, and Bacteroides fragilis). Fusidic acid is active in vitro and clinically against Mycobacterium leprae, but has only marginal activity against Mycobacterium tuberculosis.
For drug-resistant Staphylococcus aureus infections, such as pneumonia, osteomyelitis, sepsis and so on. Severe patients need intravenous administration and should be used in combination with other anti-staphylococcal drugs. Topical treatment of skin and wound infections.
| Product Name | Fusidate Sodium | ||
| Batch Number | Z20180901 | ||
| Production Date | 2018.9. 3 | ||
| Batch Quantity | 24000G | ||
| Analysis Date | 2018.9. 4 | ||
| Expiry Date | 2020.9. 2 | ||
| Certificate Date | 2018.9. 15 | ||
| Item | Test Standard | Testing Result | |
| CBD | Not less than (NLT) 99.5% 99.9% | ||
| THC | Not detected | Undetected | |
| Assay | Method HPLC calculated on the anhydrous basis limit of quotation (LOQ) 0.8ppm | ||
| Appearance | White powder | White powder | |
| Identification | In the recorded chromatograms under the determination of the substance, retention time of the main peak of the solution should be consistent with the retention of time of the main peak of the reference solution | Complies | |
| Melting Point | 65~66ºC | 65.5ºC | |
| Loss on Drying | NMT 1.0% | 0.21% | |
| Residual solvents | Ethanol NMT 400ppm Heptane NMT 400ppm | 1.92ppm 256.0ppm | |
| Heavy Mental | NMT 20ppm | Complies | |
| Microbial Limite Test | Method: Plate Counting | ||
| Total aerobic bacteria count | NMT 1000cfu/g | Complies | |
| Combined molds and yeast | NMT 100cfu/g | Complies | |
| E. Coli | Not detacted per gram | Complies | |
| Salmanella | Not detacted per 10 gram | Complies | |
| Conclusion: Conform the testing result is qualified | |||
Storage: Closed container. Dry & cool. Keep away from moisture &strong light
Shelf life: 24 Months
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