Tamsulosin Impurity

Veeprho Pharmaceuticals s.r.o. is a manufacturer and supplier of Tamsulosin Impurity B, Tamsulosin Impurity E, Tamsulosin Impurity F.

We are manufacturer and supplier of all Tamsulosin impurities which is to be isolated by preparative HPLC and Lyophillized.

Veeprho Pharmaceuticals s.r.o. is the manufacturer and supplier of certified impurity of Tamsulosin.

Veeprho Pharmaceuticals s.r.o. is the manufacturer and supplier of all Tamsulosin Impurity which are acceptable to all regulatory agencies in the world, US-FDA, MHRA, MCC, WHO, Brazil, Japan.

We are manufacturer and supplier of all Tamsulosin impurity which are used for ANDA filing/DMF filing.

We are manufacturer and supplier of all impurity of Tamsulosin shall be used for genotoxic study.

We are manufacturer and supplier of Tamsulosin with characterization data along with Certificate of analysis.

Veeprho Pharmaceuticals s.r.o. is a manufacturer and supplier of all Tamsulosin USP, EP, BP pharmacopoeia impurity.

We are manufacturer and supplier of all impurity of Tamsulosin as per pharmacopoeia RRT.

Write to us on the venkat@veeprhopharma.com email id to get specific quote.

Simvastatin Impurity

We would like inform you that Veeprho Pharmaceuticals s.r.o. is a qualified vendor for certified impurity reference standards. We are manufacturer and supplier of Simvastatin impurities like to Simvastatin Impurity A, Simvastatin Impurity B, Simvastatin Impurity C, Simvastatin Impurity D (Dimer Impurity), Simvastatin Impurity F, Simvastatin Impurity G which are isolated by preparative HPLC and Lyophillized. It is acceptable to all regulatory agencies in the world like US-FDA, MHRA, MCC, WHO, Brazil and Japan. These Simvastatin impurities are also used for ANDA filling, DMF filling and genotoxic study.

We are manufacturer and supplier of

• Certified impurity of Simvastatin.
• All Simvastatin impurity which are used for ANDA filing/DMF filing.
• All Simvastatin USP, EP, BP pharmacopoeia impurity.
• All Simvastatin Impurity as per pharmacopoeia RRT.
• All Simvastatin Impurity with characterization data along with certificate of analysis (COA).
• Unknown impurity of Simvastatin with structure elucidation with help of C NMR, H NMR, MASS, CHN, HPLC data.
• Isolation of unknown impurity of Simvastatin.

We understand the importance of RRT, RF, POTENCY of impurity and most of your vendors do not understand this critical information. We are recognized for quality material manufacturer, quality documentation and quality service. We deliver material on time as per our commitment with you, we know the value of your time and we understand that your project time line depends on availability of impurity standards.

Write to us on the venkat@veeprhopharma.com email id to get specific quote.

Ropinirole Impurity

Veeprho Pharmaceuticals s.r.o. is a manufacturer and supplier of N-Hydroxy Ropinirole, Ropinirole Impurity A and Ropinirole N-Oxide.

We are manufacturer and supplier of all Ropinirole impurity which are used for ANDA filing/DMF filing.

We are manufacturer and supplier of all impurity of Ropinirole shall be used for genotoxic study.

We are manufacturer and supplier of Ropinirole with characterization data along with Certificate of analysis.

We are manufacturer and supplier of all impurity of Ropinirole as per pharmacopoeia RRT.

Veeprho Pharmaceuticals s.r.o. is a manufacturer and supplier of all Ropinirole USP, EP, BP pharmacopoeia impurity.

Bumetanide Impurity

We are glad to announce that we have recently manufactured Bumetanide Impurity. It is ready with data and is confirmed with RT, RRT and RF.

Veeprho Pharmaceuticals s.r.o. is a manufacturer and supplier of Bumetanide Impurity 5, Bumetanide Impurity 4, Bumetanide Impurity 3.

We are manufacturer and supplier of all Bumetanide impurities which is to be isolated by preparative HPLC and Lyophillized.

Veeprho Pharmaceuticals s.r.o. is the manufacturer and supplier of certified impurity of Bumetanide.

Veeprho Pharmaceuticals s.r.o. is the manufacturer and supplier of all Bumetanide Impurity which are acceptable to all regulatory agencies in the world, US-FDA, MHRA, MCC, WHO, Brazil, Japan.

Cephalexin Impurity Manufacturer and supplier by Veeprho Pharmaceuticals s.r.o.

Greetings from Veeprho Pharmaceuticals s.r.o.

We would like inform you that Veeprho Pharmaceuticals s.r.o. is a qualified vendor for certified impurity reference standards. We are manufacturer and supplier of Cephalexin impurities like to Cephalexin Impurity J, Cephalexin Impurity K, Cephalexin Phenyl Glycin Imp, Cephalexin Impurity D, Cephalexin Impurity C etc. which are isolated by preparative HPLC and Lyophillized. It is acceptable to all regulatory agencies in the world like US-FDA, MHRA, MCC, WHO, Brazil and Japan. These Cephalexin impurities are also used for ANDA filling, DMF filling and genotoxic study.

We are manufacturer and supplier of

• Certified impurity of Cephalexin.
• All Cephalexin impurity which are used for ANDA filing/DMF filing.
• All Cephalexin USP, EP, BP pharmacopoeia impurity.
• All Cephalexin Impurity as per pharmacopoeia RRT.
• All Cephalexin Impurity with characterization data along with certificate of analysis (COA).
• Unknown impurity of Cephalexin with structure elucidation with help of C NMR, H NMR, MASS, CHN, HPLC data.
• Isolation of unknown impurity of Cephalexin.

We understand the importance of RRT, RF, POTENCY of impurity and most of your vendors do not understand this critical information. We are recognized for quality material manufacturer, quality documentation and quality service. We deliver material on time as per our commitment with you, we know the value of your time and we understand that your project time line depends on availability of impurity standards.

Write to us on the venkat@veeprhopharma.com email id to get specific quote.