Candesartan Impurities | Candesartan Cilexetil EP Impurity B, E, F, H | Candesartan Impurity 1, 2, 5, 6, 7

An ISO 9001:2008

Candesartan Impurity

Veeprho Laboratories is a manufacturer and supplier of Candesartan impurities like Candesartan Cilexetil EP Impurity F / Candesartan Cilexetil N2-Ethyl Impurity / 2H-N2-Ethyl Candesartan Cilexetil / Candesartan Cilexetil USP Related Compound F / Candesartan Impurity 7, Candesartan Cilexetil EP Impurity E / Candesartan Cilexetil N1-Ethyl Analog / 1H-N1-Ethyl Candesartan Cilexetil / Candesartan N-Ethyl Impurity / Candesartan Impurity 6 / Candesartan Impurity E, Candesartan Impurity 1 / Desethylcandesartan Methylester, Candesartan Ethyl Ester Desethyl Analog / Candesartan Desethyl Ethyl Ester / Candesartan O-Desethyl Ethyl Ester / Candesartan Ethyl Ester Impurity, Candesartan Cilexetil EP Impurity B / Candesartan Cilexetil O-Desethyl analog / Candesartan Cilexetil USP Related Compound B / Candesartan Ketone Cilexetil, Candesartan Cilexetil EP Impurity H / Candesartan Cilexetil N1-Trityl Analog / N1-Trityl Candesartan Cilexetil, Candesartan Trityl Methyl Ether Impurity / Triphenylmethyl Methyl Ether / Losartan Trityl Methyl Ether Impurity / Irbesartan Trityl Methyl Ether Impurity / Candesartan Impurity 5, Candesartan N2 Trityl Impurity / N2 Trityl Candesartan, Candesartan N-Cilexetil Impurity, Candesartan N-Cilexetil Impurity, Candesartan Desethyl Methyl Ester / Candesartan O-Desethyl Methyl Ester / Candesartan desmethyl analog, Candesartan Cilexetil EP Impurity G, Candesartan Process Impurity, Candesartan Degradation Impurity, Candesartan Related Compound and Candesartan Potential Impurity. These impurities are provided with certificate of analysis along with the characterization data like NMR MASS IR and HPLC Purity. We also provide additional data like C NMR, CHN, TGA RF on request.

We are also manufacturer and supplier of all Candesartan USP, EP, BP pharmacopoeia impurities, any unknown impurity, APIs and intermediates with structure elucidation with help of C NMR, H NMR, MASS, CHN, HPLC data. On request we also manufacture and supply all impurity of Candesartan as per pharmacopoeia RRT.

We also manufacture and supply all Candesartan impurities which are to be isolated by preparative HPLC and Lyophilized.

All the Candesartan impurities are manufactured and supplied by Veeprho Laboratories are acceptable to all regulatory agencies in the world like US-FDA, MHRA, MCC, WHO, Brazil and Japan.

These Candesartan impurities are also used for ANDA filling/DMF filling and genotoxic study.

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Candesartan Impurities :-

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