Author(s): Chinmoy Kumar, Manish Kumar, Vipin Saini, Shailendra Bhatt, A. Pandurangan, Anuj Malik, Preeti Pal, Laxmi Narayan Shetty

Email(s): manish_singh17@rediffmail.com

DOI: 10.5958/0974-360X.2019.00459.1

Address: Chinmoy Kumar1, Manish Kumar1*, Vipin Saini2, Shailendra Bhatt1, A. Pandurangan1, Anuj Malik1, Preeti Pal1, Laxmi Narayan Shetty3
1M M College of Pharmacy, Markandeshwar (Deemed to be University), Mullana, Ambala-133207, Haryana
2M M University, Solan, Himachal Pradesh.
3Reginal Drugs Testing Laboratory, Ballari, Karnataka.
*Corresponding Author

Published In:   Volume - 12,      Issue - 6,     Year - 2019


Cite this article:
Chinmoy Kumar, Manish Kumar, Vipin Saini, Shailendra Bhatt, A. Pandurangan, Anuj Malik, Preeti Pal, Laxmi Narayan Shetty. Dissolution Method Development and Validation for Combination Dosage Form of Telmisartan and Nebivolol hydrochloride Tablets using , UV Spectrophotometric Method. Research J. Pharm. and Tech. 2019; 12(6): 2742-2747. doi: 10.5958/0974-360X.2019.00459.1




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RNI: CHHENG00387/33/1/2008-TC                     
DOI: 10.5958/0974-360X 


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