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74578-69-1 Ceftriaxone Sodium Ceftriaxone Sodium for Sinopharm
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Product information:
Product Name | PHARMACEUTICAL ALLOPATHIC RAW MATERIAL FOR INDUSTRY Ceftriaxone Sodium Sterile USP | |
Shelf life | 3 years | |
TEST ITEMS | SPECIFICATION | RESULT |
Description | white to yellowish-organge crystlline powder. | Almost white crystalline powder |
Identification | ||
By IR | Meets the requirements. | Complies |
By HPLC | Meets the requirements. | Complies |
Tests for sodium | It gives reaction of sodium | Positive |
Test | ||
Crystallinity | Meets the requirements. | Complies |
pH | 6.0~8.0 | 6.5 |
Impurity A | Deacetylcetotaxime lactone≤0.5% | Not Detected |
Impurity B,C | 7-Aminocephalosporanic acid≤0.5% | 0.01% |
Impurity D | Ceftriaxone triazine analog≤1.0% | 0.09% |
Impurity E | Ceftriaxone benzathiazoly oxime≤0.2% | Not Detected |
Impurity F | Deacyl ceftriaxone≤0.5% | 0.07% |
Impurity G | Ceftriaxone 3-ene isomer≤0.3% | Not Detected |
Impurity H | Ceftriaxone E-isomer≤0.5% | 0.02% |
Any individual | ≤0.2% | 0.04% |
Unknown impurity | ||
Total impurities | ≤2.5% | 0.3% |
Water(By KF) | 8.0%~11.0% | 9.3% |
Methanol | ≤0.3% | Not Detected |
≤0.5% | Not Detected | |
≤0.041% | Not Detected | |
≤0.5% | Not Detected | |
≤0.06% | Not Detected | |
≤0.5% | Not Detected | |
Partieless≥10μg/mg:NMT 6000 part/g |
660 | |
Partieless≥25μg/mg:NMT 600 part/g | ||
<0.20EU/mg | Complies | |
It complies with the test for sterlity | Complies | |
Informative | 0.54g/ml | |
Informative | 0.72g/ml | |
ASSAY | ||
Ceftriaxone on anhydrous basis | ≥795μg/mg | 932μg/mg |
Storage Condition Preserve in airtight,tamper-proof container;in a dry place at a temperature not exceeding 20℃. | ||
RESULT: THE RESULT CONFORMS TO USP38、QS-CO11014(USP)-01 |
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