Suanfarma, at the Core of a Better Life.
01 1CIPAN - COMPANHIA INDUSTRIAL PRODUTORA DE ANTIBIOTICOS, S.A. Castanheira Do Ribatejo PT
02 1KOPRAN RESEARCH LABORATORIES LIMITED Mumbai IN
03 2OLON S.P.A. Rodano IT
01 3Lymecycline
02 1Lymecycline, Type 2
01 1India
02 2Italy
03 1Spain
01 4Valid
Certificate Number : R1-CEP 2010-239 - Rev 02
Status : Valid
Issue Date : 2023-02-09
Type : Chemical
Substance Number : 1654
Certificate Number : CEP 2020-040 - Rev 01
Status : Valid
Issue Date : 2024-12-18
Type : Chemical
Substance Number : 1654
Certificate Number : R1-CEP 2016-186 - Rev 01
Status : Valid
Issue Date : 2023-04-26
Type : Chemical
Substance Number : 1654
Certificate Number : R0-CEP 2023-172 - Rev 00
Status : Valid
Issue Date : 2023-08-09
Type : Chemical
Substance Number : 1654
A Lymecycline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lymecycline, including repackagers and relabelers. The FDA regulates Lymecycline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lymecycline 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 Lymecycline manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lymecycline supplier is an individual or a company that provides Lymecycline active pharmaceutical ingredient (API) or Lymecycline finished formulations upon request. The Lymecycline suppliers may include Lymecycline API manufacturers, exporters, distributors and traders.
click here to find a list of Lymecycline suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lymecycline CEP of the European Pharmacopoeia monograph is often referred to as a Lymecycline Certificate of Suitability (COS). The purpose of a Lymecycline CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Lymecycline EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Lymecycline to their clients by showing that a Lymecycline CEP has been issued for it. The manufacturer submits a Lymecycline CEP (COS) as part of the market authorization procedure, and it takes on the role of a Lymecycline CEP holder for the record. Additionally, the data presented in the Lymecycline CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Lymecycline DMF.
A Lymecycline CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Lymecycline 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 Lymecycline suppliers with CEP (COS) on PharmaCompass.
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