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01 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
02 1FRESENIUS KABI IPSUM S.R.L. Cassina de’ Pecchi IT
03 1PARABOLIC DRUGS LIMITED Panchkula District IN
04 1Ribbon S.r.l. Milano IT
05 1Sandoz Industrial Products S.A. Les Franqueses Del Vallès ES
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01 2Dicloxacillin sodium monohydrate
02 2Dicloxacillin sodium monohydrate, Powder and compacted
03 1Dicloxacillin sodium monohydrate, sterile
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01 1Germany
02 2India
03 2Italy
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01 2Valid
02 1Withdrawn by EDQM Failure to CEP procedure
03 2Withdrawn by Holder
Dicloxacillin Sodium Monohydrate
Certificate Number : CEP 2010-177 - Rev 03
Status : Valid
Issue Date : 2023-11-30
Type : Chemical
Substance Number : 663
Dicloxacillin Sodium Monohydrate, Powder And Com...
Certificate Number : CEP 2002-036 - Rev 09
Status : Valid
Issue Date : 2025-03-21
Type : Chemical
Substance Number : 663
Dicloxacillin Sodium Monohydrate
Certificate Number : R0-CEP 2011-052 - Rev 00
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2013-01-11
Type : Chemical
Substance Number : 663
Dicloxacillin Sodium Monohydrate, Sterile
Certificate Number : R1-CEP 1996-092 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2002-02-18
Type : Chemical
Substance Number : 663
Dicloxacillin Sodium Monohydrate, Powder And Com...
Certificate Number : R1-CEP 1996-023 - Rev 04
Status : Withdrawn by Holder
Issue Date : 2016-07-25
Type : Chemical
Substance Number : 663
99
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A DSSTox_CID_28928 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_CID_28928, including repackagers and relabelers. The FDA regulates DSSTox_CID_28928 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_CID_28928 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A DSSTox_CID_28928 supplier is an individual or a company that provides DSSTox_CID_28928 active pharmaceutical ingredient (API) or DSSTox_CID_28928 finished formulations upon request. The DSSTox_CID_28928 suppliers may include DSSTox_CID_28928 API manufacturers, exporters, distributors and traders.
click here to find a list of DSSTox_CID_28928 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DSSTox_CID_28928 CEP of the European Pharmacopoeia monograph is often referred to as a DSSTox_CID_28928 Certificate of Suitability (COS). The purpose of a DSSTox_CID_28928 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of DSSTox_CID_28928 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of DSSTox_CID_28928 to their clients by showing that a DSSTox_CID_28928 CEP has been issued for it. The manufacturer submits a DSSTox_CID_28928 CEP (COS) as part of the market authorization procedure, and it takes on the role of a DSSTox_CID_28928 CEP holder for the record. Additionally, the data presented in the DSSTox_CID_28928 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the DSSTox_CID_28928 DMF.
A DSSTox_CID_28928 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. DSSTox_CID_28928 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 DSSTox_CID_28928 suppliers with CEP (COS) on PharmaCompass.
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