01 MINAKEM Dunkerque FR (1)
02 CORAL DRUGS PRIVATE LIMITED New Delhi IN (1)
03 FERMION OY Espoo FI (2)
04 ASPEN OSS B.V. Oss NL (2)
05 AARTI PHARMALABS LIMITED Mulund (W), Mumbai IN (1)
06 Farmabios SpA Gropello Cairoli IT (2)
07 Hubei Gedian Humanwell Pharmaceutical Co., Ltd. E-Zhou CN (1)
08 AVIK PHARMACEUTICAL LIMITED Vapi IN (1)
09 CIPLA LIMITED Mumbai IN (2)
10 CURIA SPAIN S.A.U. Boecillo ES (2)
11 HENAN LIHUA PHARMACEUTICAL CO., LTD. Anyang CN (1)
12 Industriale Chimica S.R.L. Saronno IT (1)
13 NEWCHEM S.p.A. Milano IT (2)
14 STERLING S.p.A. Solomeo Di Corciano IT (2)
15 SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN (1)
16 TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL (3)
17 TIANJIN TIANYAO PHARMACEUTICALS CO., LTD. Tianjin CN (1)
01 Budesonide (14)
02 Budesonide, Budesonide ZS (1)
03 Budesonide, Codes 201680 and 2016112 (1)
04 Budesonide, Micronised (1)
05 Budesonide, Micronised, grades 21, 22 and 23 (1)
06 Budesonide, Micronised, non-micronised (3)
07 Budesonide, Process 2, non-micronised and micronised (1)
08 Budesonide, Process II, micronised (1)
09 Budesonide, Sterile (1)
10 Budesonide, T Process (1)
11 Budesonide, micronised (1)
01 China (3)
02 Finland (2)
03 France (1)
04 India (6)
05 Israel (3)
06 Italy (7)
07 Netherlands (2)
08 Spain (2)
01 Expired (1)
02 Valid (25)
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.
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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.
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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.
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A Prestwick3_000518 CEP of the European Pharmacopoeia monograph is often referred to as a Prestwick3_000518 Certificate of Suitability (COS). The purpose of a Prestwick3_000518 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Prestwick3_000518 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Prestwick3_000518 to their clients by showing that a Prestwick3_000518 CEP has been issued for it. The manufacturer submits a Prestwick3_000518 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Prestwick3_000518 CEP holder for the record. Additionally, the data presented in the Prestwick3_000518 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Prestwick3_000518 DMF.
A Prestwick3_000518 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Prestwick3_000518 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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We have 17 companies offering Prestwick3_000518
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