含量测定(Assay): 含量测定(HPLC):以无水/干燥品计,norethisterone enanthate (50 mg/mL) and estradiol valerate (5 mg/mL) combined含量为90.0–110.0% of the labeled strength for each component,符合相应药典专论限度要求。
Clarity of Solution: 溶液澄清,几乎不含可见异物,oily injectable solution, free from visible particulate matter,按药典澄清度标准以目视法评估。
Color of Solution: 溶液颜色不深于参比标准色(pale yellow oily solution typical of the castor-oil vehicle),通过与药典标准比色液比对进行验证。
杂质谱: 单个未知杂质≤0.10%,总杂质≤0.5%,per cGMP/ISO-certified release testing at Montage Laboratories Pvt. Ltd.,通过经验证的HPLC/UPLC方法进行控制。
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