LOAD MORE
You're viewed all 12 products
Cefdinir
References
FAQ's
References
- Takaya, Takao; Takasugi, Hisashi; Masugi, Takashi; Yamanaka, Hideaki; Kawabata, Kohji, 7-Substituted-3-vinyl-3-cephem compounds and processes for production of the same, Fujisawa Pharmaceutical Co., Ltd., Japan, US4559334A, December 17, 1985
- Okamoto, Yoshihiko; Itoh, Kohji; Namiki, Yoshihiro; Matsushita, Junichi; Fujioka, Mamoru; Yasuda, Tsutomu, Method development for the determination of cefdinir and its related substances by high-performance liquid chromatography, Journal of Pharmaceutical and Biomedical Analysis, Volume: 14, Issue: 6, Pages: 739-748, 1996
Frequently Asked Questions
What is the effect of impurities on the shelf life of Cefdinir?
The effect of impurities on the shelf life of Cefdinir depends on the specific impurity class and the storage conditions of the drug. Impurities reduce the drug's potency and efficacy by degradation. Further, their presence in the drug product may also accelerate the breakdown of the drug, leading to a shorter shelf life.
What analytical techniques help to monitor Cefdinir impurities during its synthesis?
Analytical techniques such as HPLC and LC-MS help monitor Cefdinir impurities during manufacturing.
Which solvent is for the analysis of Cefdinir impurities?
DMSO is a solvent to analyze Cefdinir and its impurities.
What are the temperature conditions required to store Cefdinir impurities?
Cefdinir impurities should be stored at a controlled room temperature between 2-8 ⁰C or as indicated on the Certificate of Analysis (CoA).
Note: Products protected by valid patents by a manufacturer are not offered for sale in countries having patent protection. The sale of such products constitutes a patent infringement, and its liability is at the buyer's risk.