Market Place
Coral's API range includes Corticosteroids, Antihistamines. Hormones and Antineoplastics. 
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01 M/s. Coral Drugs Ltd., (1)
02 M/s. Vamsi Lab Ltd., (1)
03 M/s. Aarti Pharmalabs Limited (1)
04 M/s Melody Healthcare Pvt Ltd (1)
05 M/s. Cipla Ltd (1)
06 M/s. MSN Laboratories Pvt. Ltd., (1)
07 M/s. Mylan Lab Ltd. (1)
08 M/sMSN Laboratories Private Limited (1)
01 Formoterol Fumarate (USP) (1)
02 Formoterol Fumarate Dihydrate (BP/EP/USP/IP) (1)
03 Formoterol Fumarate Dihydrate (BP/Ph. Eur./USP) (1)
04 Formoterol Fumarate Dihydrate (INH) (1)
05 Formoterol Fumarate Dihydrate BP/EP (1)
06 Formoterol Fumarate Dihydrate EP (1)
07 Formoterol Fumarate Dihydrate EP/Formoterol Fumarate USP (1)
08 Formoterol Fumarate USP/Formoterol Fumarate Dihydrate EP/BP (1)
01 WC-0009 (1)
02 WC-0021 (1)
03 WC-0021n (1)
04 WC-0099 (1)
05 WC-0144 (1)
06 WC-0155 (1)
07 WC-0157 (1)
08 WC-0227 (1)
01 India (8)
Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs. 
Iran Expo
Not Confirmed
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PharmaCompass offers a list of Formoterol Fumarate 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 Formoterol Fumarate manufacturer or Formoterol Fumarate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Formoterol Fumarate manufacturer or Formoterol Fumarate supplier.
PharmaCompass also assists you with knowing the Formoterol Fumarate API Price utilized in the formulation of products. Formoterol Fumarate API Price is not always fixed or binding as the Formoterol Fumarate Price is obtained through a variety of data sources. The Formoterol Fumarate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dulera manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dulera, including repackagers and relabelers. The FDA regulates Dulera manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dulera 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 Dulera manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dulera supplier is an individual or a company that provides Dulera active pharmaceutical ingredient (API) or Dulera finished formulations upon request. The Dulera suppliers may include Dulera API manufacturers, exporters, distributors and traders.
click here to find a list of Dulera suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dulera written confirmation (Dulera WC) is an official document issued by a regulatory agency to a Dulera manufacturer, verifying that the manufacturing facility of a Dulera active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Dulera APIs or Dulera finished pharmaceutical products to another nation, regulatory agencies frequently require a Dulera WC (written confirmation) as part of the regulatory process.
click here to find a list of Dulera suppliers with Written Confirmation (WC) on PharmaCompass.
We have 7 companies offering Dulera
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