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Minakem offers CDMO services for API & HPAPI, generics, regulatory expertise, track record performance & FDA & GMP certifications. 
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01 Minakem Dunkerque Production (2)
02 VAMSI LABS LIMITED. (1)
03 Coral Drugs Private Limited (1)
04 Aspen Oss B.V. (1)
05 Aarti Pharmalabs Limited (1)
06 Farmabios S.p.A. (2)
07 Hubei Gedian Humanwell Pharmaceutical Co., Ltd (1)
08 AX Pharmaceutical Corp (1)
09 Amphastar Nanjing Pharmaceuticals, Inc. (1)
10 AstraZeneca AB (2)
11 Cipla Ltd. (1)
12 Curia Spain, S.A.U. (2)
13 Darmerica, LLC (1)
14 Fagron Inc (1)
15 Industriale Chimica s.r.l. (3)
16 KALCHEM INTERNATIONAL INC (1)
17 LETCO MEDICAL, LLC (1)
18 Medisca Inc. (1)
19 NEWCHEM SPA (1)
20 Professional Compounding Centers of America dba PCCA (1)
21 Sicor S.p.a. (1)
22 Sicor S.r.l. (2)
23 Sicor de Mexico S.A. de C.V (1)
24 Spectrum Laboratory Products, Inc. (1)
25 Sterling S.p.A. (2)
26 Symbiotica Speciality Ingredients Sdn. Bhd. (1)
27 Willow Birch Pharma, Inc. (1)
28 Xenex Laboratories Inc (1)
01 BUDESONIDE (5)
02 BUDESONIDE MICRONIZED (4)
03 Budesonide (20)
04 Budesonide Micronised Co-Suspension APN (1)
05 Budesonide Micronized (5)
06 budesonide (1)
01 Canada (2)
02 China (1)
03 France (2)
04 Germany (2)
05 India (4)
06 Italy (9)
07 Malaysia (1)
08 Mexico (1)
09 Netherlands (2)
10 U.S.A (9)
11 United Kingdom (3)
Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs. 
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PharmaCompass offers a list of Budesonide 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 Budesonide manufacturer or Budesonide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Budesonide manufacturer or Budesonide supplier.
PharmaCompass also assists you with knowing the Budesonide API Price utilized in the formulation of products. Budesonide API Price is not always fixed or binding as the Budesonide Price is obtained through a variety of data sources. The Budesonide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Prestwick3_000518 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prestwick3_000518, including repackagers and relabelers. The FDA regulates Prestwick3_000518 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prestwick3_000518 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 Prestwick3_000518 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Prestwick3_000518 supplier is an individual or a company that provides Prestwick3_000518 active pharmaceutical ingredient (API) or Prestwick3_000518 finished formulations upon request. The Prestwick3_000518 suppliers may include Prestwick3_000518 API manufacturers, exporters, distributors and traders.
click here to find a list of Prestwick3_000518 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Prestwick3_000518 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Prestwick3_000518 API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Prestwick3_000518 as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Prestwick3_000518 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Prestwick3_000518 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Prestwick3_000518 suppliers with NDC on PharmaCompass.
We have 28 companies offering Prestwick3_000518
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