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. Perai 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 1AURISCO PHARMACEUTICAL CO., LTD. Tiantai CN
06 1GlaxoSmithKline Research & Development Limited Brentford GB
07 1GlaxoSmithKline Research & Development Limited London GB
08 1HENAN LIHUA PHARMACEUTICAL CO., LTD. Anyang CN
09 1Pharmacia & Upjohn Company Kalamazoo US
10 1SM BIOMED SDN BHD Sungai Petani MY
11 1SYMBIOTEC PHARMALAB LIMITED Indore IN
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01 7Betamethasone valerate
02 4Betamethasone valerate, Micronised
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01 2China
02 1Israel
03 1Italy
04 2Malaysia
05 1Spain
06 1U.S.A
07 2United Kingdom
08 1Blank
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01 1Expired
02 8Valid
03 1Withdrawn by EDQM GMP non-compliance
04 1Withdrawn by Holder
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 : R1-CEP 2008-215 - Rev 00
Status : Valid
Issue Date : 2015-06-26
Type : Chemical
Substance Number : 811
Betamethasone Valerate, Micronised
Certificate Number : R1-CEP 2002-078 - Rev 03
Status : Valid
Issue Date : 2021-03-22
Type : Chemical
Substance Number : 811
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 2003-095 - Rev 05
Status : Valid
Issue Date : 2025-02-26
Type : Chemical
Substance Number : 811
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 2003-022 - Rev 02
Status : Valid
Issue Date : 2021-08-24
Type : Chemical
Substance Number : 811
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Certificate Number : CEP 2021-120 - Rev 02
Status : Valid
Issue Date : 2025-09-15
Type : Chemical
Substance Number : 811

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Betamethasone Valerate, Micronised
Certificate Number : CEP 2002-219 - Rev 09
Status : Valid
Issue Date : 2024-10-25
Type : Chemical
Substance Number : 811

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Certificate Number : R0-CEP 2021-509 - Rev 00
Status : Valid
Issue Date : 2022-07-13
Type : Chemical
Substance Number : 811

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Certificate Number : R0-CEP 2001-307 - Rev 00
Status : Expired
Issue Date : 2002-07-29
Type : TSE
Substance Number : 811

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Certificate Number : R1-CEP 1999-118 - Rev 00
Status : Withdrawn by EDQM GMP non-compliance
Issue Date : 2009-08-12
Type : Chemical
Substance Number : 811

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Corporate PDF

Betamethasone Valerate, Micronised
Certificate Number : CEP 2008-307 - Rev 01
Status : Valid
Issue Date : 2026-04-02
Type : Chemical
Substance Number : 811

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PharmaCompass offers a list of Betamethasone Valerate 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 Valerate manufacturer or Betamethasone Valerate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Betamethasone Valerate manufacturer or Betamethasone Valerate supplier.
A Otomax (Veterinary) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Otomax (Veterinary), including repackagers and relabelers. The FDA regulates Otomax (Veterinary) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Otomax (Veterinary) 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 Otomax (Veterinary) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Otomax (Veterinary) supplier is an individual or a company that provides Otomax (Veterinary) active pharmaceutical ingredient (API) or Otomax (Veterinary) finished formulations upon request. The Otomax (Veterinary) suppliers may include Otomax (Veterinary) API manufacturers, exporters, distributors and traders.
click here to find a list of Otomax (Veterinary) suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Otomax (Veterinary) CEP of the European Pharmacopoeia monograph is often referred to as a Otomax (Veterinary) Certificate of Suitability (COS). The purpose of a Otomax (Veterinary) CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Otomax (Veterinary) EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Otomax (Veterinary) to their clients by showing that a Otomax (Veterinary) CEP has been issued for it. The manufacturer submits a Otomax (Veterinary) CEP (COS) as part of the market authorization procedure, and it takes on the role of a Otomax (Veterinary) CEP holder for the record. Additionally, the data presented in the Otomax (Veterinary) CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Otomax (Veterinary) DMF.
A Otomax (Veterinary) CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Otomax (Veterinary) 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 Otomax (Veterinary) suppliers with CEP (COS) on PharmaCompass.
We have 9 companies offering Otomax (Veterinary)
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