Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
01 1Laboratory Ofichem B. V.
02 1Dr. Paul Lohmann GmbH & Co. KGaA
03 1Fuji Chemical Industry Co., Ltd.
04 1Purity Chemicals, S. L.
01 2Zinc Acetate Dihydrate
02 1Zinc acetate 2-hydrate
03 1Zinc acetate hydrate (for manufacturing only)
01 1Germany
02 1Japan
03 1Netherlands
04 1Spain
Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
Registration Number : 304MF10017
Registrant's Address : Heembadweg 5, 9561 CZ Ter apel, The Netherlands
Initial Date of Registration : 2022-01-20
Latest Date of Registration : 2024-02-14
Registration Number : 304MF10096
Registrant's Address : Hauptstrasse 2 D-31860 Emmerthal Germany
Initial Date of Registration : 2022-07-06
Latest Date of Registration : 2022-07-06
Zinc acetate hydrate (for manufacturing only)
Registration Number : 306MF10011
Registrant's Address : 55 Yokohoonji, Kamiichi-cho, Nakaniikawa-gun, Toyama Prefecture
Initial Date of Registration : 2024-01-17
Latest Date of Registration : 2024-01-17
Registration Number : 304MF10105
Registrant's Address : Avda. Tren Expresso, Parcelas 82-84 PO Box, 4 34200 Venta de Banos, Palencia, Spain
Initial Date of Registration : 2022-07-27
Latest Date of Registration : 2023-05-10
A Zinc Acetate Dihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zinc Acetate Dihydrate, including repackagers and relabelers. The FDA regulates Zinc Acetate Dihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zinc Acetate Dihydrate 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 Zinc Acetate Dihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zinc Acetate Dihydrate supplier is an individual or a company that provides Zinc Acetate Dihydrate active pharmaceutical ingredient (API) or Zinc Acetate Dihydrate finished formulations upon request. The Zinc Acetate Dihydrate suppliers may include Zinc Acetate Dihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Zinc Acetate Dihydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Zinc Acetate Dihydrate Drug Master File in Japan (Zinc Acetate Dihydrate JDMF) empowers Zinc Acetate Dihydrate API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Zinc Acetate Dihydrate JDMF during the approval evaluation for pharmaceutical products. At the time of Zinc Acetate Dihydrate JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Zinc Acetate Dihydrate suppliers with JDMF on PharmaCompass.
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