Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
01 1LABORATORIUM OFICHEM B.V. Ter Apel NL
02 1CIPLA LIMITED Mumbai IN
03 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
01 3Pamidronate disodium pentahydrate
01 2India
02 1Netherlands
01 2Valid
02 1Withdrawn by Holder
Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
Pamidronate Disodium Pentahydrate
Certificate Number : CEP 2017-203 - Rev 01
Status : Valid
Issue Date : 2023-11-17
Type : Chemical
Substance Number : 1779
Pamidronate Disodium Pentahydrate
Certificate Number : R1-CEP 2007-082 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2014-07-28
Type : Chemical
Substance Number : 1779
Pamidronate Disodium Pentahydrate
Certificate Number : R1-CEP 2007-312 - Rev 02
Status : Valid
Issue Date : 2015-06-18
Type : Chemical
Substance Number : 1779
A Disodium Pamidronate Pentahydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Disodium Pamidronate Pentahydrate, including repackagers and relabelers. The FDA regulates Disodium Pamidronate Pentahydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Disodium Pamidronate Pentahydrate 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 Disodium Pamidronate Pentahydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Disodium Pamidronate Pentahydrate supplier is an individual or a company that provides Disodium Pamidronate Pentahydrate active pharmaceutical ingredient (API) or Disodium Pamidronate Pentahydrate finished formulations upon request. The Disodium Pamidronate Pentahydrate suppliers may include Disodium Pamidronate Pentahydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Disodium Pamidronate Pentahydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Disodium Pamidronate Pentahydrate CEP of the European Pharmacopoeia monograph is often referred to as a Disodium Pamidronate Pentahydrate Certificate of Suitability (COS). The purpose of a Disodium Pamidronate Pentahydrate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Disodium Pamidronate Pentahydrate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Disodium Pamidronate Pentahydrate to their clients by showing that a Disodium Pamidronate Pentahydrate CEP has been issued for it. The manufacturer submits a Disodium Pamidronate Pentahydrate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Disodium Pamidronate Pentahydrate CEP holder for the record. Additionally, the data presented in the Disodium Pamidronate Pentahydrate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Disodium Pamidronate Pentahydrate DMF.
A Disodium Pamidronate Pentahydrate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Disodium Pamidronate Pentahydrate 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 Disodium Pamidronate Pentahydrate suppliers with CEP (COS) on PharmaCompass.
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