Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.
01 1MINAKEM Dunkerque FR
02 1CORAL DRUGS PRIVATE LIMITED New Delhi IN
03 2Farmabios SpA Gropello Cairoli IT
04 2ASPEN OSS B.V. Oss NL
05 3FERMION OY Espoo FI
06 1AARTI PHARMALABS LIMITED Mulund (W), Mumbai IN
07 3TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
08 1AVIK PHARMACEUTICAL LIMITED Vapi IN
09 2CIPLA LIMITED Mumbai IN
10 2CURIA SPAIN S.A.U. Boecillo ES
11 1HENAN LIHUA PHARMACEUTICAL CO., LTD. Anyang CN
12 1Hubei Gedian Humanwell Pharmaceutical Co., Ltd. Ezhou City CN
13 1Industriale Chimica S.R.L. Saronno IT
14 2NEWCHEM S.p.A. Milano IT
15 1SHAKTI LIFESCIENCE PRIVATE LIMITED Mumbai IN
16 2STERLING S.p.A. Solomeo Di Corciano IT
17 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
18 1TIANJIN TIANYAO PHARMACEUTICALS CO., LTD. Tianjin CN
01 15Budesonide
02 1Budesonide, Budesonide ZS
03 1Budesonide, Codes 201680 and 2016112
04 1Budesonide, Micronised
05 1Budesonide, Micronised, grades 21, 22 and 23
06 3Budesonide, Micronised, non-micronised
07 1Budesonide, Process 2, non-micronised and micronised
08 1Budesonide, Process 3, micronised
09 1Budesonide, Process II, micronised
10 1Budesonide, Sterile
11 1Budesonide, T Process
12 1Budesonide, micronised
01 3China
02 3Finland
03 1France
04 7India
05 3Israel
06 7Italy
07 2Netherlands
08 2Spain
01 1Expired
02 27Valid
Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.
Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.
Budesonide, Micronised, Non-micronised
Certificate Number : R1-CEP 2010-190 - Rev 03
Status : Valid
Issue Date : 2020-06-09
Type : Chemical
Substance Number : 1075
Certificate Number : R1-CEP 2016-020 - Rev 00
Status : Valid
Issue Date : 2022-11-15
Type : Chemical
Substance Number : 1075
Certificate Number : R1-CEP 2000-051 - Rev 02
Status : Valid
Issue Date : 2010-05-04
Type : Chemical
Substance Number : 1075
Certificate Number : R0-CEP 2021-491 - Rev 01
Status : Valid
Issue Date : 2023-02-10
Type : Chemical
Substance Number : 1075
Budesonide, Micronised, Non-micronised
Certificate Number : R0-CEP 2020-341 - Rev 00
Status : Valid
Issue Date : 2022-02-22
Type : Chemical
Substance Number : 1075
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Certificate Number : R1-CEP 2006-295 - Rev 04
Status : Valid
Issue Date : 2022-10-14
Type : Chemical
Substance Number : 1075
Certificate Number : R0-CEP 2019-266 - Rev 00
Status : Valid
Issue Date : 2022-03-09
Type : Chemical
Substance Number : 1075
Budesonide, Micronised, Grades 21, 22 And 23
Certificate Number : R1-CEP 2005-174 - Rev 01
Status : Valid
Issue Date : 2017-07-25
Type : Chemical
Substance Number : 1075
Certificate Number : R1-CEP 2016-043 - Rev 01
Status : Valid
Issue Date : 2023-02-10
Type : Chemical
Substance Number : 1075
Budesonide, Process 2, Non-micronised And Micron...
Certificate Number : CEP 2023-192 - Rev 00
Status : Valid
Issue Date : 2023-09-26
Type : Chemical
Substance Number : 1075
A Symbicort manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Symbicort, including repackagers and relabelers. The FDA regulates Symbicort manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Symbicort 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 Symbicort manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Symbicort supplier is an individual or a company that provides Symbicort active pharmaceutical ingredient (API) or Symbicort finished formulations upon request. The Symbicort suppliers may include Symbicort API manufacturers, exporters, distributors and traders.
click here to find a list of Symbicort suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Symbicort CEP of the European Pharmacopoeia monograph is often referred to as a Symbicort Certificate of Suitability (COS). The purpose of a Symbicort CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Symbicort EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Symbicort to their clients by showing that a Symbicort CEP has been issued for it. The manufacturer submits a Symbicort CEP (COS) as part of the market authorization procedure, and it takes on the role of a Symbicort CEP holder for the record. Additionally, the data presented in the Symbicort CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Symbicort DMF.
A Symbicort CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Symbicort CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Symbicort suppliers with CEP (COS) on PharmaCompass.
We have 18 companies offering Symbicort
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