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Neuland Laboratories- A dedicated 100% API provider. 
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01 M/s. Neuland Laboratories Ltd (1)
02 M/s Teva API India Private Limited (1)
03 GVK Biosciences Private Limited (1)
04 M/s GVK Biosciences Private Limited (1)
05 M/s Glenmark Life Sciences Limited (2)
06 M/s Hetero Labs Ltd (1)
07 M/s Saptagir Laboratories (1)
08 M/s. Hetro Labs Limited (1)
09 M/s. Ind- Swift Laboratories Limited (1)
10 M/s. Lupin Ltd (1)
11 M/s. Mylan Laboratories Ltd., (1)
12 M/s. Richter Themis Medicare (I) Pvt. Ltd., (1)
13 M/sMSN Laboratories Private Limited (1)
14 Micro Labs Limited (1)
01 Ezetimibe (1)
02 Ezetimibe (IH) (4)
03 Ezetimibe IH (3)
04 Ezetimibe IH, USP (1)
05 Ezetimibe IH/USP (2)
06 Ezetimibe USP (3)
07 Ezitimibe (IH) (1)
01 WC-0002 (1)
02 WC-0003 (1)
03 WC-0021n (1)
04 WC-0037 (1)
05 WC-0041 (1)
06 WC-0057n (1)
07 WC-0112 (1)
08 WC-0118 (1)
09 WC-0124 (1)
10 WC-0201 (1)
11 WC-0225A7 (1)
12 WC-0310 (1)
13 WC-0365 (1)
14 WC-0467A1 (1)
15 WC-0472A1 (1)
01 India (15)
15
PharmaCompass offers a list of Ezetimibe API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Ezetimibe manufacturer or Ezetimibe supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ezetimibe manufacturer or Ezetimibe supplier.
PharmaCompass also assists you with knowing the Ezetimibe API Price utilized in the formulation of products. Ezetimibe API Price is not always fixed or binding as the Ezetimibe Price is obtained through a variety of data sources. The Ezetimibe Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A VYTORIN manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of VYTORIN, including repackagers and relabelers. The FDA regulates VYTORIN manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. VYTORIN API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of VYTORIN manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A VYTORIN supplier is an individual or a company that provides VYTORIN active pharmaceutical ingredient (API) or VYTORIN finished formulations upon request. The VYTORIN suppliers may include VYTORIN API manufacturers, exporters, distributors and traders.
click here to find a list of VYTORIN suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A VYTORIN written confirmation (VYTORIN WC) is an official document issued by a regulatory agency to a VYTORIN manufacturer, verifying that the manufacturing facility of a VYTORIN active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting VYTORIN APIs or VYTORIN finished pharmaceutical products to another nation, regulatory agencies frequently require a VYTORIN WC (written confirmation) as part of the regulatory process.
click here to find a list of VYTORIN suppliers with Written Confirmation (WC) on PharmaCompass.
We have 12 companies offering VYTORIN
Get in contact with the supplier of your choice:
