Powder: | Yes |
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Customized: | Non-Customized |
Certification: | GMP, HSE, ISO 9001, USP |
Suitable for: | Elderly, Children, Adult |
State: | Solid |
Purity: | >99% |
Samples: |
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Customization: |
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Product Name | Ranitidine Hcl |
Package | 25KG Drum |
Description | White to pale yellow, crystalline practically odorless powder |
Identification |
A.The IR absorption spectrum of the test specimen comply with that of the corresponding USP Reference Standard
B.Absorptivities at 229nm and 315nm ,do not differ by more than 3.0%
C. A solution of it meets the requirements of Chloride. |
pH | Should be 4.5~6.0 |
Loss on drying | ≤0.75% |
Residue on ignition | ≤0.1% |
Chromatographic purity | Ranitidine related Compound B: ≤0.5% Any other impurity: ≤0.3% The sum of all impurities: ≤1.0% |
Organic volatile impurities | Meet the requirements |
Residual solvents | Alcohol: ≤0.5% |
Assay | Assay (Dried basis C13H22N4O3S·HCl 97.5%~102%) |
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