What you should know about Veeprho Laboratories Private Limited
VEEPRHO is GMP and ISO certified manufacturer and supplier of Impurity Reference Standards with FDA approved scientist and top notch technology. We are involved in the research, development, and distribution of synthesized impurities, metabolites, intermediates, and API’s with custom synthesis.
Our global network is comprised with our headquarters in Czech Republic EU, manufacturing and R&D facilities in India, as well as distribution offices in US, and United Kingdom equipped to provide immediate support within all time zones.
Our vision is to provide high quality products around the world to support the Pharmaceutical Industry in making compounds free of errors and establishing a community with risk free medical treatment. Reference Standards are the supporting blocks of the medical industry, and our initiative is to contribute the best we can to enable the functioning of proper and reliable treatment.
High regulations, product availability, as well as, the passion of thinking innovatively fuel our mission at the VEEPRHO. We have also strategically developed our brand to ensure utmost quality in our products and regulatory compliances, with a cost-efficient plan, which can help our customers meet their necessities in a productive manner, ultimately allowing us to provide our products/services at competitive rates. This is possible by our cutting-edge technology, and by bringing out the best capabilities of our highly qualified team.
VEEPRHO is an emerging, research-based global pharmaceutical company with diverse combination of skills, resources, and capabilities that provide the platform to perform effectively in today's rapidly changing healthcare environment.
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Products
Doxycycline EP Impurity F /
2-Acetyl-2-Decarbamoyldoxycycline, Doxycycline EP Impurity D / 4-Epi 6-Epi
Doxycycline, Doxycycline EP Impurity B / Methacycline Impurity, Doxycycline EP
Impurity C / 4-Epidoxycycline / Doxycycline Related Compound C, Canagliflozin Hydroperoxide
Impurity, Clopidogrel EP Impurity D / Clopidogrel BP Impurity D, Tranexamic
Acid EP Impurity A, Loratadine EP Impurity E / Loratadine Alkene Isomer, Rifaximin
EP Impurity G, Acyclovir EP Impurity O, Domperidone EP Impurity D, Acetazolamide
EP Impurity F/ Acetazolamide Dimer Impurity, Atorvastatin Epoxy Tetrahydrofuran
Analog, Atorvastatin FX1 Impurity / Atorvastatin Cyclic Fluorophenyl (Cyclo FP)
/ Atorvastatin Epoxy Pyrrolooxazin 7-Hydroxy analog, Atorvastatin FXA Impurity
/ Atorvastatin 6-Hydroxy analog / Atorvastatin Cyclo IP, Atorvastatin
Pyrrolidone Analog (USP) / Atorvastatin Lactam, Azithromycin EP Impurity C, Azithromycin
EP Impurity O, Bupropion S,R,R,-Thiomorpholine derivative, Bupropion
S,S,S-Thiomorpholine Derivative, Colesevelam Impurity 2 / Aminoquat, Colesevelam
Impurity 3 / Decylaminoquat, Colesevelam Impurity 4 / Aminodihexylquat, 17
Desoxy of Dexamethasone, 17-Oxo Dexamethasone / 17-Keto Dexamethasone, 17β-Carboxy-17-Desoxy
Dexamethasone, 21 Dehydro Dexamethasone, 9-Desfluoro-11-Keto Dexamethasone, Dexamethasone
-17-Ketone, Dexamethasone Acetate EP Impurity D, Dexamethasone Acetate EP
Impurity I, Dexamethasone EP Impurity B, Dexamethasone EP impurity D /
Dexamethasone 9,11-β Epoxide, Dexamethasone EP Impurity G, Dexamethasone EP
Impurity K / Δ7,9 (11)-Dexamethasone, Dexamethasone Impurity 7, Dexamethasone
EP Impurity I / Dexamethasone-9(11)-α-Epoxide, Dexamethasone-Δ
17,20 21-Aldehyde, Emtricitabin Diastereomer Impurity, Emtricitabine Carboxylic
Acid Impurity, Emtricitabine Enantiomer Impurity, Emtricitabine S-Fluorouracil
Analogue / Emtricitabine Hydroxy Impurity, Emtricitabine Sulfoxide Impurity, Erythromycin
EP Impurity B, Erythromycin EP Impurity C, Erythromycin EP Impurity D / Anhydro
erythromycin A, Erythromycin EP Impurity E / Erythromycin A Enol Ether, Erythromycin
EP Impurity F / Pseudoerythromycin A Enol Ether, Erythromycin EP Impurity H /
Erythromycin A N-oxide / Erythromycin In house G impurity, Erythromycin EP
Impurity I, Erythromycin Ethylsuccinate EP Impurity G, Fulvestrant EP Impurity
A / Fulvestrant Beta Isomer, Fulvestrant EP Impurity B / Fulvestrant Sulfone, Fulvestrant
EP Impurity C / Fulvestrant Extended, Fulvestrant EP Impurity D / Fulvestrant
Sterol Dimer Impurity, Fulvestrant EP Impurity E / Delta 6,7 Fulvestrant
Impurity, Fulvestrant EP Impurity F / 6-Keto Fulvestrant, 17-Keto Fulvestrant, Hydrochlorothiazide
EP Impurity C / Hydrochlorothiazide Dimer, Hydroxychloroquine 3-Bromo Impurity,
Hydroxychloroquine Acid, Hydroxychloroquine Aminopentyl, Hydroxychloroquine
Dimer, Hydroxychloroquine EP Impurity A / Hydroxychloroquine N-Oxide, Hydroxychloroquine
EP Impurity B (Free Base), Hydroxychloroquine EP Impurity B (Na Salt) /
Hydroxychloroquine O-Sulfate, Hydroxychloroquine EP Impurity C, Hydroxychloroquine
EP Impurity D, Hydroxychloroquine EP Impurity E, Hydroxychloroquine EP Impurity
F, Hydroxychloroquine EP Impurity G / Amodiaquine Dichloro Impurity, Hydroxychloroquine
O acetate, Hydroxychloroquine R-isomer Impurity, Hydroxychloroquine S-isomer
Impurity, Irbesartan Nitroso Impurity, Irbesartan Nitroso Spiro Impurity, Levothyroxine
Acetamide Impurity / Levothyroxine T4-Acetamide (USP), Levothyroxine Beta
Hydroxy, Levothyroxine EP Impurity A / Liothyronine Acid, Levothyroxine EP
Impurity B, Levothyroxine EP Impurity C, Levothyroxine EP Impurity D, Levothyroxine
EP Impurity F, Levothyroxine Impurity K / 3,3’,5’-Triiodo-L-Thyronine, Levothyroxine
N-Acetyl Impurity / N-Acetyl-T4 (USP), Levothyroxine N-Formyl Impurity /
N-Formyl-T4 (USP), Levothyroxine N-Methylamide, Levothyroxine T4 Amine O-Methyl
/ Levothyroxine T4 Amine O-Methyl / Levothyroxine
O-Methyl-Tetraiodothyroethyla
Services
Impurity Reference Standards Supplier, Impurity standards Manufacturer, pharmaceutical impurity manufacturer, Impurity Reference Standards Manufacturer, Isolation Purification of known and unknown Impurity, Certified Impurity Standards Manufacturer, Manufacturer of Pharmaceutical Impurity, Impurity Isolation & Purification Service, Synthesis of Impurity
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