Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
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01 1Farmak A.S. Olomouc CZ
02 1C-SQUARED PHARMA LIMITED Cork IE
03 1CENTAUR PHARMACEUTICALS PRIVATE LIMITED Mumbai IN
04 1CURIA WISCONSIN, INC. Grafton US
05 1FDC Limited Mumbai IN
06 1INDOCO REMEDIES LIMITED Mumbai IN
07 1MAITHRI DRUGS PRIVATE LIMITED Bonthapally Village IN
08 1MICRO LABS LIMITED Bengaluru IN
09 1Medichem, S.A. Sant Joan Despí ES
10 1PIRAMAL PHARMA LIMITED Digwal Village IN
11 1SYMED LABS LIMITED Hyderabad IN
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01 11Brimonidine tartrate
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01 1Czech Republic
02 6India
03 1Ireland
04 1Spain
05 2U.S.A
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01 11Valid
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Certificate Number : CEP 2014-331 - Rev 03
Status : Valid
Issue Date : 2024-03-06
Type : Chemical
Substance Number : 2760
Certificate Number : CEP 2022-451 - Rev 00
Status : Valid
Issue Date : 2024-11-25
Type : Chemical
Substance Number : 2760
Certificate Number : R1-CEP 2015-265 - Rev 00
Status : Valid
Issue Date : 2023-01-24
Type : Chemical
Substance Number : 2760
Certificate Number : R0-CEP 2020-123 - Rev 00
Status : Valid
Issue Date : 2022-06-13
Type : Chemical
Substance Number : 2760
Certificate Number : CEP 2014-180 - Rev 01
Status : Valid
Issue Date : 2024-03-20
Type : Chemical
Substance Number : 2760
Certificate Number : R0-CEP 2021-507 - Rev 00
Status : Valid
Issue Date : 2023-07-04
Type : Chemical
Substance Number : 2760
Certificate Number : R1-CEP 2013-353 - Rev 00
Status : Valid
Issue Date : 2019-04-24
Type : Chemical
Substance Number : 2760
Certificate Number : CEP 2019-335 - Rev 02
Status : Valid
Issue Date : 2024-04-18
Type : Chemical
Substance Number : 2760
Certificate Number : R1-CEP 2015-052 - Rev 01
Status : Valid
Issue Date : 2022-01-07
Type : Chemical
Substance Number : 2760
Certificate Number : R0-CEP 2018-124 - Rev 00
Status : Valid
Issue Date : 2020-05-14
Type : Chemical
Substance Number : 2760
19
PharmaCompass offers a list of Brimonidine Tartrate 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 Brimonidine Tartrate manufacturer or Brimonidine Tartrate supplier for your needs.
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PharmaCompass also assists you with knowing the Brimonidine Tartrate API Price utilized in the formulation of products. Brimonidine Tartrate API Price is not always fixed or binding as the Brimonidine Tartrate Price is obtained through a variety of data sources. The Brimonidine Tartrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A QOLIANA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of QOLIANA, including repackagers and relabelers. The FDA regulates QOLIANA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. QOLIANA 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 QOLIANA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A QOLIANA supplier is an individual or a company that provides QOLIANA active pharmaceutical ingredient (API) or QOLIANA finished formulations upon request. The QOLIANA suppliers may include QOLIANA API manufacturers, exporters, distributors and traders.
click here to find a list of QOLIANA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A QOLIANA CEP of the European Pharmacopoeia monograph is often referred to as a QOLIANA Certificate of Suitability (COS). The purpose of a QOLIANA CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of QOLIANA EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of QOLIANA to their clients by showing that a QOLIANA CEP has been issued for it. The manufacturer submits a QOLIANA CEP (COS) as part of the market authorization procedure, and it takes on the role of a QOLIANA CEP holder for the record. Additionally, the data presented in the QOLIANA CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the QOLIANA DMF.
A QOLIANA CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. QOLIANA 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 QOLIANA suppliers with CEP (COS) on PharmaCompass.
We have 11 companies offering QOLIANA
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