01 1Alta Laboratories Ltd Khopoli IN
02 1Bayer Hispania, S.L. La Felguera ES
03 1Chimprod SA Oradea RO
04 1Industria Quimica Andina & Cia. S.A. Bogota D.C CO
05 1Jilin Pharmaceutical Co Ltd Jilin City CN
06 1SHANDONG XINHUA PHARMACEUTICAL CO., LTD. Zibo CN
07 1The Andhra Sugars Limited Tanuku IN
08 1WP MANNHEIM GMBH Mannheim DE
01 6Acetylsalicylic acid
02 1Acetylsalicylic acid, Crystals 7010/7011, fines 7012, granules 7017/7018, granular powder 7028, PR powder 7029
03 1Acetylsalicylic acid, Type 100/300, Type 100/500, Type 300/500, Type 300/800, Type 500/800
01 1China
02 2Germany
03 3India
04 1Romania
05 1U.S.A
01 1Expired
02 3Valid
03 3Withdrawn by EDQM Failure to CEP procedure
04 1Withdrawn by Holder
Acetylsalicylic Acid, Crystals 7010/7011, Fines ...
Certificate Number : R1-CEP 2000-013 - Rev 01
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2007-09-11
Type : Chemical
Substance Number : 309
Certificate Number : R1-CEP 2001-292 - Rev 04
Status : Valid
Issue Date : 2011-04-15
Type : Chemical
Substance Number : 309
Certificate Number : R1-CEP 1994-014 - Rev 02
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2008-09-17
Type : Chemical
Substance Number : 309
Certificate Number : R0-CEP 2001-399 - Rev 01
Status : Expired
Issue Date : 2006-05-17
Type : Chemical
Substance Number : 309
Certificate Number : R0-CEP 2006-195 - Rev 00
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2008-12-16
Type : Chemical
Substance Number : 309
Certificate Number : R1-CEP 2001-210 - Rev 05
Status : Valid
Issue Date : 2016-11-14
Type : Chemical
Substance Number : 309
Certificate Number : R1-CEP 2000-042 - Rev 04
Status : Valid
Issue Date : 2021-04-20
Type : Chemical
Substance Number : 309
Acetylsalicylic Acid, Type 100/300, Type 100/500...
Certificate Number : R1-CEP 2003-084 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2010-08-17
Type : Chemical
Substance Number : 309
A Solprin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Solprin, including repackagers and relabelers. The FDA regulates Solprin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Solprin 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 Solprin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Solprin supplier is an individual or a company that provides Solprin active pharmaceutical ingredient (API) or Solprin finished formulations upon request. The Solprin suppliers may include Solprin API manufacturers, exporters, distributors and traders.
click here to find a list of Solprin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Solprin CEP of the European Pharmacopoeia monograph is often referred to as a Solprin Certificate of Suitability (COS). The purpose of a Solprin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Solprin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Solprin to their clients by showing that a Solprin CEP has been issued for it. The manufacturer submits a Solprin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Solprin CEP holder for the record. Additionally, the data presented in the Solprin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Solprin DMF.
A Solprin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Solprin 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 Solprin suppliers with CEP (COS) on PharmaCompass.
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