TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1TAPI Czech Industries s. r. o.
01 1Methyl Ergo cytometry down maleate "Teva"
01 1Israel
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Methylergometrine Maleate (Teva)
Registration Number : 224MF10233
Registrant's Address : Ostravska 305/29, Komarov, 747 70 Opava, Czech Republic
Initial Date of Registration : 2012-12-18
Latest Date of Registration : 2024-04-18
A Methylergonovine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methylergonovine, including repackagers and relabelers. The FDA regulates Methylergonovine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methylergonovine 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 Methylergonovine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Methylergonovine supplier is an individual or a company that provides Methylergonovine active pharmaceutical ingredient (API) or Methylergonovine finished formulations upon request. The Methylergonovine suppliers may include Methylergonovine API manufacturers, exporters, distributors and traders.
click here to find a list of Methylergonovine 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 Methylergonovine Drug Master File in Japan (Methylergonovine JDMF) empowers Methylergonovine 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 Methylergonovine JDMF during the approval evaluation for pharmaceutical products. At the time of Methylergonovine 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 Methylergonovine suppliers with JDMF on PharmaCompass.
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