Development and validation of a generic RP‐HPLC PDA method for the simultaneous separation and quantification of active ingredients in cold and cough medicines
- DOI
- 10.1002/bmc.4641
- Published
- 2019-08-08
- Container
- Biomedical Chromatography
- Publisher
- Wiley
- Open access
- unknown
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Cite this work
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
Source records
- crossref · retrieved 2026-09-25T07:10:24.917Z