Azelastine Impurities

Azelastine Impurities : https://www.veeprhopharma.com/Azelastine-Impurity-Manufacturer-Supplier.php



Azelastine EP Impurity A
Azelastine EP Impurity B
Azelastine EP Impurity C
Azelastine EP Impurity D
Azelastine EP Impurity E

Amoxicillin Impurities

Amoxicillin Impurities :

Amoxicillin Related Compound A/Amoxicillin EP Impurity A
Amoxicillin Related Compound B/Amoxicillin EP Impurity B
Amoxicillin Related Compound C/Amoxicillin EP Impurity C
Amoxicillin Related Compound D/Amoxicillin EP Impurity D
Amoxicillin Related Compound F/Amoxicillin EP Impurity F
Amoxicillin Related Compound I/Amoxicillin EP Impurity I
Amoxicillin Related Compound G/Amoxicillin EP Impurity G
Amoxicillin Related Compound H/Amoxicillin EP Impurity H
Amoxicillin Related Compound J/Amoxicillin EP Impurity J

For more details visit : - https://www.veeprhopharma.com/Amoxicillin-impurity-manufacturer-supplier.php

Clobazam EP Impurity D

Clobazam EP Impurity D

Propafenone Impurity A

Propafenone Impurity A

Amlodipine Related Compound C / Amlodipine EP Impurity G

Amlodipine Related Compound C / Amlodipine EP Impurity G 

Salmeterol Impurities by veeprhopharma

All Fluvastatin Impurities are Successfully Manufactured in our R&D Center.

Veeprho is multinational company. Veeprho Pharmaceutical s.r.o is a manufacturer and supplier of Fluvastatin impurities like Fluvastatin Anti-isomer and Fluvastatin Methyl Ester. These hashtag#impurities are provided with certificate of analysis (COA) along with the characterization data like NMR MASS IR, HPLC Purity and structure elucidation report. All hashtag#fluvastatin impurities which are isolated by preparative HPLC and Lyophilized. These are high quality impurity standards, our clients are used it in ANDA and DMF Dossier submission. These all Veeprho make impurity standards are acceptable to all regulatory agency in the world including US-FDA. We are producing and selling it from 2010, now it is Global company, having office in USA, EU, and India. Reason to purchase impurity standards from Veeprho is faster delivery, quality documentation, quality material and most economical in the world. https://lnkd.in/fpGjSnd

All Pioglitazone Impurities are Successfully Manufactured in our R&D Center.

Veeprho Pharmaceutical s.r.o is a manufacturer and supplier of Pioglitazone hashtag#impurities like N-Alkyl Pioglitazone / Pioglitazone EP Impurity C, Pioglitazone Didehydro Impurity / Pioglitazone EP Impurity B, Hydroxy Pioglitazone (CAS No. 146062-44-4), Pioglitazone EP Impurity A / 5-Hydroxy Pioglitazone (CAS No. 625853-74-9), Pioglitazone EP Impurity D, 1-Hydroxy Pioglitazone (M4-Metabolite), Pioglitazone Bromo impurity and Pioglitazone Amine Impurity. These impurities are provided with certificate of analysis (COA) along with the characterization data like NMR MASS IR, HPLC Purity and structure elucidation report. All hashtag#pioglitazone impurities which are isolated by preparative HPLC and Lyophilized. These are high quality impurity standards, our clients are used it in ANDA and DMF Dossier submission. These all Veeprho make impurity standards are acceptable to all regulatory agency in the world including US-FDA. https://lnkd.in/fxrhG9T

Diphenhydramine Impurity D

Diphenhydramine Impurity D

Catalogue No : VL177004

CAS No. : 91-01-0

IUPAC Name : Diphenylmethanol(benzhydrol)

For more details visit : https://www.veeprhopharma.com/diphenhydramine-impurity-d-cas-no-91-01-0.php

Rosuvastatin Z-Isomer

Rosuvastatin Z-Isomer

IUPAC Name : (3R,5R.6E)-7-[4-(4-fluorophenyl)-2-(N-methylmethanesulfonamido)-6-(propan-2-yl)pyrimidine-5-yl]-3-dihydroxyhept-6-enoic acid calcium salt

Catalogue No : VL127011

For more details visit : https://www.veeprhopharma.com/Rosuvastatin-Impurity-Manufacturer-Supplier.php

Rosuvastatin Impurity F

Rosuvastatin Impurity F / Rosuvastatin Related Compound C

IUPAC Name : tert-butyl 2-((4R,6S)-6-((E)-2-(4-(4-fluorophenyl)-6-isopropyl-2-(Nmethylmethylsulfonamido)

Catalogue No : VL127004

For more details visit : https://www.veeprhopharma.com/Rosuvastatin-Impurity-Manufacturer-Supplier.php

Oxytetracycline EP Impurity C

Oxytetracycline EP Impurity C / 2-acetyl-2- decarbamoyloxytetracyclin

Catalogue No : VL1960004

Category : Oxytetracycline

CAS No. : 6542-44-5

IUPAC Name : (4S,4aR,5S,5aR,6S,12aS)-2-acetyl-4-(dimethylamino)- 3,5,6,10,12,12a-hexahydroxy-6-methyl-4a,5a,6,12a-tetrahydrotetracene -1,11(4H,5H)-dion

Molecular Weight : 459.15 g/mol

Molecular Formula : C23H₂5NO9

For more details visit following link :

https://www.veeprholabs.com/cas-no-6542-44-5-oxytetracycline-ep-impurity-c.php

All Capecitabine Impurities are Successfully Manufactured in our R&D Center.

Veeprho is multinational company.

Veeprho Pharmaceutical s.r.o is a manufacturer and supplier of Capecitabine impurities like Capecitabine Related Compound A, Capecitabine Related Compound B and Capecitabine Related Compound C. These impurities are provided with certificate of analysis (COA) along with the characterization data like NMR MASS IR, HPLC Purity and structure elucidation report. All Capecitabine impurities which are isolated by preparative HPLC and Lyophilized. These are high quality impurity standards, our clients are used it in ANDA and DMF Dossier submission. These all Veeprho make impurity standards are acceptable to all regulatory agency in the world including US-FDA.

We are producing and selling it from 2010, now it is Global company, having office in USA, EU, and India.

Reason to purchase impurity standards from Veeprho is faster delivery, quality documentation, quality material and most economical in the world.

For more details visit : https://www.veeprhopharma.com/Capecitabine-Impurity-Manufacturer-Supplier.php