Market Place
Minakem offers CDMO services for API & HPAPI, generics, regulatory expertise, track record performance & FDA & GMP certifications. 
X
Please Wait
Applying Filters...
01 Minakem (1)
02 Coral Drugs Private Limited (1)
03 Aspen API (1)
04 Aarti Pharmalabs (1)
05 Axplora (2)
06 Hubei Gedian Humanwell Pharmaceutical (1)
07 Amphastar Pharmaceuticals (1)
08 Apotex Pharmachem (1)
09 AstraZeneca (1)
10 Cipla (1)
11 Curia (2)
12 Henan Lihua Pharmaceutical (1)
13 Industriale Chimica s.r.l. (2)
14 NEWCHEM SPA (1)
15 Sterling Spa (1)
16 Sun Pharmaceutical Industries Limited (1)
17 Teva API (2)
18 Tianjin Tianyao Pharmaceuticals Co., Ltd. (1)
01 BUDESONIDE (10)
02 BUDESONIDE MICRONIZED (3)
03 BUDESONIDE MICRONIZED STERILE (1)
04 BUDESONIDE STERILE MICRONIZED (1)
05 BUDESONIDE USP (6)
06 BUDESONIDE USP BULK API (1)
01 Canada (1)
02 China (3)
03 France (1)
04 Germany (2)
05 India (4)
06 Israel (2)
07 Italy (4)
08 Netherlands (1)
09 U.S.A (3)
10 United Kingdom (1)
01 Active (21)
02 Inactive (1)
01 Complete (15)
02 Blank (7)
Iran Expo
Not Confirmed
Contact SupplierIran Expo
Not Confirmed
Contact Supplier
50
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.
A Prestwick3_000518 DMF (Drug Master File) is a document detailing the whole manufacturing process of Prestwick3_000518 active pharmaceutical ingredient (API) in detail. Different forms of Prestwick3_000518 DMFs exist exist since differing nations have different regulations, such as Prestwick3_000518 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Prestwick3_000518 DMF submitted to regulatory agencies in the US is known as a USDMF. Prestwick3_000518 USDMF includes data on Prestwick3_000518's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Prestwick3_000518 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Prestwick3_000518 suppliers with USDMF on PharmaCompass.
We have 18 companies offering Prestwick3_000518
Get in contact with the supplier of your choice:
