Symbiotica delivers high-quality APIs through advanced R&D, GMP-certified manufacturing, & trusted global pharmaceutical partnerships.

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01 1SYMBIOTICA SPECIALITY INGREDIENTS SDN. BHD. Butterworth MY
02 1FARMABIOS S.p.A Gropello Cairoli IT
03 1TAPI NL B.V. Amsterdam NL
04 1CURIA SPAIN S.A.U. Boecillo ES
05 1HENAN LIHUA PHARMACEUTICAL CO., LTD. Anyang CN
06 1SYMBIOTEC PHARMALAB LIMITED Indore IN
07 1TARO PHARMACEUTICAL INDUSTRIES, LTD. Haifa IL
08 1TIANJIN TIANYAO PHARMACEUTICALS CO., LTD. Tianjin CN
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01 5Betamethasone dipropionate
02 3Betamethasone dipropionate, Micronised
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01 2China
02 1Israel
03 1Italy
04 1Malaysia
05 1Spain
06 2Blank
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01 8Valid
Symbiotica delivers high-quality APIs through advanced R&D, GMP-certified manufacturing, & trusted global pharmaceutical partnerships.
Symbiotica delivers high-quality APIs through advanced R&D, GMP-certified manufacturing, & trusted global pharmaceutical partnerships.
Certificate Number : CEP 2011-005 - Rev 02
Status : Valid
Issue Date : 2024-12-23
Type : Chemical
Substance Number : 809
Betamethasone Dipropionate, Micronised
Certificate Number : R1-CEP 2003-232 - Rev 03
Status : Valid
Issue Date : 2023-02-08
Type : Chemical
Substance Number : 809
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : CEP 2000-223 - Rev 09
Status : Valid
Issue Date : 2025-08-08
Type : Chemical
Substance Number : 809
Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
Certificate Number : R1-CEP 2002-031 - Rev 03
Status : Valid
Issue Date : 2021-08-24
Type : Chemical
Substance Number : 809
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Certificate Number : R0-CEP 2020-418 - Rev 00
Status : Valid
Issue Date : 2022-05-24
Type : Chemical
Substance Number : 809

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Certificate Number : CEP 2022-342 - Rev 00
Status : Valid
Issue Date : 2024-04-30
Type : Chemical
Substance Number : 809

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Betamethasone Dipropionate, Micronised
Certificate Number : CEP 2012-079 - Rev 01
Status : Valid
Issue Date : 2026-04-01
Type : Chemical
Substance Number : 809

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Betamethasone Dipropionate, Micronised
Certificate Number : CEP 2018-018 - Rev 04
Status : Valid
Issue Date : 2026-02-23
Type : Chemical
Substance Number : 809

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PharmaCompass offers a list of Betamethasone Dipropionate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Betamethasone Dipropionate manufacturer or Betamethasone Dipropionate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Betamethasone Dipropionate manufacturer or Betamethasone Dipropionate supplier.
A TACLONEX manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of TACLONEX, including repackagers and relabelers. The FDA regulates TACLONEX manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. TACLONEX 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 TACLONEX manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A TACLONEX supplier is an individual or a company that provides TACLONEX active pharmaceutical ingredient (API) or TACLONEX finished formulations upon request. The TACLONEX suppliers may include TACLONEX API manufacturers, exporters, distributors and traders.
click here to find a list of TACLONEX suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A TACLONEX CEP of the European Pharmacopoeia monograph is often referred to as a TACLONEX Certificate of Suitability (COS). The purpose of a TACLONEX CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of TACLONEX EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of TACLONEX to their clients by showing that a TACLONEX CEP has been issued for it. The manufacturer submits a TACLONEX CEP (COS) as part of the market authorization procedure, and it takes on the role of a TACLONEX CEP holder for the record. Additionally, the data presented in the TACLONEX CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the TACLONEX DMF.
A TACLONEX CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. TACLONEX 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 TACLONEX suppliers with CEP (COS) on PharmaCompass.
We have 6 companies offering TACLONEX
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