Bayer AG manufactures innovative APIs and pharmaceutical formulations across diverse therapeutic areas.
01 1BAYER AG Leverkusen DE
02 1Becton, Dickinson and Company Sparks US
03 1CIPLA LIMITED Mumbai IN
04 5GEDEON RICHTER PLC. Budapest HU
05 3INDUSTRIALE CHIMICA S.R.L. Saronno IT
06 2NEWCHEM S.p.A. Milano IT
07 1STERLING CHEMICAL MALTA LTD. Birzebbugia MT
08 1STERLING S.p.A. Solomeo Di Corciano IT
09 1SYMBIOTEC PHARMALAB LIMITED Indore IN
10 1ZHEJIANG XIANJU JUNYE PHARMACEUTICAL CO., LTD. Xianju CN
01 5Drospirenone
02 1Drospirenone, Code 202900
03 1Drospirenone, Fine Form
04 1Drospirenone, Micronised (micro 15)
05 2Drospirenone, Micronised, non-micronised
06 1Drospirenone, Micronised, non-micronised NW
07 2Drospirenone, Process 2
08 1Drospirenone, Process 2 micronized
09 1Drospirenone, Process I
10 1Drospirenone, Process I micronised
11 1Dubos Medium, Product codes: 215334, 230910, 237310, 237510, 238510 and 295697
01 1China
02 1Germany
03 5Hungary
04 1India
05 7Italy
06 1U.S.A
07 1Blank
01 16Valid
02 1Withdrawn by Holder
Bayer AG manufactures innovative APIs and pharmaceutical formulations across diverse therapeutic areas.
Bayer AG manufactures innovative APIs and pharmaceutical formulations across diverse therapeutic areas.
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 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
Drospirenone, Process 2 Micronized
Certificate Number : R0-CEP 2022-279 - Rev 00
Status : Valid
Issue Date : 2022-12-01
Type : Chemical
Substance Number : 2404
Drospirenone, Process I Micronised
Certificate Number : CEP 2024-461 - Rev 00
Status : Valid
Issue Date : 2025-01-20
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
Drospirenone, Micronised, Non-micronised
Certificate Number : R1-CEP 2015-247 - Rev 01
Status : Valid
Issue Date : 2023-08-01
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 : CEP 2023-457 - Rev 00
Status : Valid
Issue Date : 2025-06-18
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
100
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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, and COA 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, and COA 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.
We have 8 companies offering ANGELIQ
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