01 1SIGMA-ALDRICH ISRAEL Ltd.
01 1Dactinomycin USP
01 1U.S.A
Registration Number : 221MF10187
Registrant's Address : 13 Kiryat Mada Street, Har Hotzvim Industrial Park Jerusalem, 97770 ISRAEL
Initial Date of Registration : 2009-08-13
Latest Date of Registration : 2017-02-13
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PharmaCompass offers a list of Dactinomycin 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 Dactinomycin manufacturer or Dactinomycin supplier for your needs.
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PharmaCompass also assists you with knowing the Dactinomycin API Price utilized in the formulation of products. Dactinomycin API Price is not always fixed or binding as the Dactinomycin Price is obtained through a variety of data sources. The Dactinomycin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lyovac cosmegen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lyovac cosmegen, including repackagers and relabelers. The FDA regulates Lyovac cosmegen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lyovac cosmegen 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 Lyovac cosmegen supplier is an individual or a company that provides Lyovac cosmegen active pharmaceutical ingredient (API) or Lyovac cosmegen finished formulations upon request. The Lyovac cosmegen suppliers may include Lyovac cosmegen API manufacturers, exporters, distributors and traders.
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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 Lyovac cosmegen Drug Master File in Japan (Lyovac cosmegen JDMF) empowers Lyovac cosmegen 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 Lyovac cosmegen JDMF during the approval evaluation for pharmaceutical products. At the time of Lyovac cosmegen JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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