Development and validation of a generic RP‐HPLC PDA method for the simultaneous separation and quantification of active ingredients in cold and cough medicines

Thirupathi Dongala, Naresh Kumar Katari, Ashok Kumar Palakurthi, Sreekantha B. Jonnalagadda

Open source

DOI
10.1002/bmc.4641
Published
2019-08-08
Container
Biomedical Chromatography
Publisher
Wiley
Open access
unknown

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BibTeX

@article{allodium:10.1002/bmc.4641,
  title = {Development and validation of a generic RP‐HPLC PDA method for the simultaneous separation and quantification of active ingredients in cold and cough medicines},
  author = {Thirupathi Dongala and Naresh Kumar Katari and Ashok Kumar Palakurthi and Sreekantha B. Jonnalagadda},
  year = {2019},
  journal = {Biomedical Chromatography},
  doi = {10.1002/bmc.4641},
  url = {https://doi.org/10.1002/bmc.4641}
}

RIS

TY  - JOUR
TI  - Development and validation of a generic RP‐HPLC PDA method for the simultaneous separation and quantification of active ingredients in cold and cough medicines
AU  - Thirupathi Dongala
AU  - Naresh Kumar Katari
AU  - Ashok Kumar Palakurthi
AU  - Sreekantha B. Jonnalagadda
PY  - 2019
JO  - Biomedical Chromatography
DO  - 10.1002/bmc.4641
UR  - https://doi.org/10.1002/bmc.4641
ER  - 

APA

Dongala, T., Katari, N. K., Palakurthi, A. K., & Jonnalagadda, S. B. (2019). Development and validation of a generic RP‐HPLC PDA method for the simultaneous separation and quantification of active ingredients in cold and cough medicines. Biomedical Chromatography. https://doi.org/10.1002/bmc.4641

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