Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
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01 1SYMBIOTEC PHARMALAB PRIVATE LIMITED Indore IN
02 1BAYER AG Leverkusen DE
03 1CIPLA LIMITED Mumbai IN
04 1CURIA SPAIN S.A.U. Boecillo ES
05 4GEDEON RICHTER PLC Budapest HU
06 3Industriale Chimica S.R.L. Saronno IT
07 2NEWCHEM S.p.A. Milano IT
08 1STERLING S.p.A. Solomeo Di Corciano IT
09 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
10 1ZHEJIANG XIANJU JUNYE PHARMACEUTICAL CO., LTD. Xianju CN
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01 7Drospirenone
02 1Drospirenone, Fine Form
03 1Drospirenone, Micronised (micro 15)
04 2Drospirenone, Micronised, non-micronised
05 1Drospirenone, Micronised, non-micronised NW
06 2Drospirenone, Process 2
07 1Drospirenone, Process 2 micronized
08 1Drospirenone, Process I
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01 1China
02 1Germany
03 4Hungary
04 2India
05 1Israel
06 6Italy
07 1Spain
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01 15Valid
02 1Withdrawn by Holder
Drospirenone, Micronised, Non-micronised
Certificate Number : CEP 2018-118 - Rev 01
Status : Valid
Issue Date : 2024-09-11
Type : Chemical
Substance Number : 2404
Drospirenone, Micronised (micro 15)
Certificate Number : R1-CEP 2009-070 - Rev 02
Status : Valid
Issue Date : 2022-07-27
Type : Chemical
Substance Number : 2404
Certificate Number : R1-CEP 2012-049 - Rev 01
Status : Valid
Issue Date : 2021-08-25
Type : Chemical
Substance Number : 2404
Certificate Number : R1-CEP 2009-402 - Rev 00
Status : Valid
Issue Date : 2015-06-08
Type : Chemical and TSE
Substance Number : 2404
Certificate Number : R0-CEP 2022-278 - Rev 01
Status : Valid
Issue Date : 2023-07-31
Type : Chemical
Substance Number : 2404
Certificate Number : CEP 2022-506 - Rev 00
Status : Valid
Issue Date : 2025-01-10
Type : Chemical
Substance Number : 2404
Drospirenone, Micronised, Non-micronised NW
Certificate Number : R0-CEP 2021-370 - Rev 01
Status : Valid
Issue Date : 2023-07-21
Type : Chemical
Substance Number : 2404
Certificate Number : R1-CEP 2009-193 - Rev 00
Status : Valid
Issue Date : 2015-08-20
Type : Chemical
Substance Number : 2404
Certificate Number : R1-CEP 2010-014 - Rev 01
Status : Valid
Issue Date : 2022-01-04
Type : Chemical
Substance Number : 2404
Certificate Number : R1-CEP 2012-143 - Rev 00
Status : Valid
Issue Date : 2018-11-05
Type : Chemical
Substance Number : 2404
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PharmaCompass offers a list of Drospirenone 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 Drospirenone manufacturer or Drospirenone supplier for your needs.
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PharmaCompass also assists you with knowing the Drospirenone API Price utilized in the formulation of products. Drospirenone API Price is not always fixed or binding as the Drospirenone Price is obtained through a variety of data sources. The Drospirenone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ANGELIQ manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ANGELIQ, including repackagers and relabelers. The FDA regulates ANGELIQ manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ANGELIQ 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 ANGELIQ manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ANGELIQ supplier is an individual or a company that provides ANGELIQ active pharmaceutical ingredient (API) or ANGELIQ finished formulations upon request. The ANGELIQ suppliers may include ANGELIQ API manufacturers, exporters, distributors and traders.
click here to find a list of ANGELIQ suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A ANGELIQ CEP of the European Pharmacopoeia monograph is often referred to as a ANGELIQ Certificate of Suitability (COS). The purpose of a ANGELIQ CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of ANGELIQ EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of ANGELIQ to their clients by showing that a ANGELIQ CEP has been issued for it. The manufacturer submits a ANGELIQ CEP (COS) as part of the market authorization procedure, and it takes on the role of a ANGELIQ CEP holder for the record. Additionally, the data presented in the ANGELIQ CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the ANGELIQ DMF.
A ANGELIQ CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. ANGELIQ 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 ANGELIQ suppliers with CEP (COS) on PharmaCompass.
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