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Introduction
Product Name | Enrofloxacin Hydrochloride |
Brand Name | Faithful |
Purity | 99% |
MF | C19H22FN3O3 |
Appearance | White Powder |
Test Method | HPLC |
Function
1. Dogs and Cats
The product is indicated in the treatment of bacterial infections of the alimentary, respiratory and urogenital tracts, skin, secondary wound infections and otitis externa where clinical experience, supported where possible by sensitivity testing of the causal organism, indicates enrofloxacin as the drug of choice.
2. Cattle
Diseases of the respiratory and alimentary tract of bacterial or mycoplasmal origin (e.g. pasteurellosis, mycoplasmosis, coli-bacillosis, coli-septicaemia and salmonellosis) and secondary bacterial infections subsequent to viral conditions (e.g. viral pneumonia) where clinical experience, supported where possible by sensitivity testing of the causal organism, indicates enrofloxacin as the drug of choice.
3. Pigs
Diseases of the respiratory and alimentary tract of bacterial or mycoplasmal origin (e.g. pasteurellosis, actinobacillosis, mycoplasmosis, coli-bacillosis, coli-septicaemia and salmonellosis) and mulifactorial diseases such as atrophic rhinitis and enzootic pneumonia, where clinical experience, supported where possible by sensitivity testing of the causal organism, indicates enrofloxacin as the drug of choice
Specification
tems | Specifications | Results |
Character | White or almost white crystalline powder;odorless | white crystelline powder, odorless |
Melting point | 242~246°C | 243.4~244.3°C |
Identification | 1) IR spectra is consistent with CRS | complies |
2) The retention time of the major peak in the chromatogram of the assay preparation corresponds to that in the chromatogram of the standard preparation, as obtained in the assay | complies | |
Appearance of solution | colorless and clear liquid | colorless and clear liquid |
Related substances | individual impurity≤1.0% | 0.24% |
Total impuirties ≤2.0% | 0.70% | |
Loss on ignition | ≤0.5% | 0.32% |
Residue on ignition | ≤0.1% | 0.05% |
Heavy metals | Not more than 10 parts per million | Less than 10 parts per million |
Assay | Not less than 98.0% of C18H14F3N3O6S(On dried basis) | 99.40% |
Conclusion: | Complies with Ponazuril Enterprise Standard |