01 1AMSA S.P.A. - ANONIMA MATERIE SINTETICHE & AFFINI Como IT
02 1ICROM S.R.L. Concorezzo IT
03 1IPCA LABORATORIES LIMITED Mumbai IN
04 1LIAOYUAN SILVER EAGLE PHARMACEUTICAL CO., LTD. Liaoyuan City CN
01 4Metoclopramide Hydrochloride monohydrate
01 1China
02 1India
03 2Italy
01 4Valid
Metoclopramide Hydrochloride Monohydrate
Certificate Number : CEP 2023-100 - Rev 00
Status : Valid
Issue Date : 2024-03-28
Type : Chemical
Substance Number : 674
Metoclopramide Hydrochloride Monohydrate
Certificate Number : R1-CEP 2015-304 - Rev 00
Status : Valid
Issue Date : 2021-05-20
Type : Chemical
Substance Number : 674
Metoclopramide Hydrochloride Monohydrate
Certificate Number : CEP 2004-075 - Rev 05
Status : Valid
Issue Date : 2024-03-12
Type : Chemical
Substance Number : 674
Metoclopramide Hydrochloride Monohydrate
Certificate Number : CEP 2015-082 - Rev 01
Status : Valid
Issue Date : 2024-03-08
Type : Chemical
Substance Number : 674
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PharmaCompass offers a list of Metoclopramide Hydrochloride 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 Metoclopramide Hydrochloride manufacturer or Metoclopramide Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Metoclopramide Hydrochloride manufacturer or Metoclopramide Hydrochloride supplier.
PharmaCompass also assists you with knowing the Metoclopramide Hydrochloride API Price utilized in the formulation of products. Metoclopramide Hydrochloride API Price is not always fixed or binding as the Metoclopramide Hydrochloride Price is obtained through a variety of data sources. The Metoclopramide Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Metozolv ODT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Metozolv ODT, including repackagers and relabelers. The FDA regulates Metozolv ODT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Metozolv ODT 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 Metozolv ODT supplier is an individual or a company that provides Metozolv ODT active pharmaceutical ingredient (API) or Metozolv ODT finished formulations upon request. The Metozolv ODT suppliers may include Metozolv ODT API manufacturers, exporters, distributors and traders.
click here to find a list of Metozolv ODT suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Metozolv ODT CEP of the European Pharmacopoeia monograph is often referred to as a Metozolv ODT Certificate of Suitability (COS). The purpose of a Metozolv ODT CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Metozolv ODT EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Metozolv ODT to their clients by showing that a Metozolv ODT CEP has been issued for it. The manufacturer submits a Metozolv ODT CEP (COS) as part of the market authorization procedure, and it takes on the role of a Metozolv ODT CEP holder for the record. Additionally, the data presented in the Metozolv ODT CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Metozolv ODT DMF.
A Metozolv ODT CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Metozolv ODT 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 Metozolv ODT suppliers with CEP (COS) on PharmaCompass.
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