01 2Procos S. p. A.
02 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
01 1Labetalol hydrochloride
02 1Labetalol hydrochloride "Teva 2"
03 1Labetalol hydrochloride GR
01 3Italy
Registration Number : 224MF10101
Registrant's Address : Via Matteotti 249,28062 CAMERI (NOVARA)/ITALY
Initial Date of Registration : 2012-05-25
Latest Date of Registration : 2012-05-25
Registration Number : 218MF10992
Registrant's Address : Via Matteotti 249,28062 CAMERI(NOVARA)/ITALY
Initial Date of Registration : 2006-12-18
Latest Date of Registration : 2006-12-18
Labetalol hydrochloride (Teva 2)
Registration Number : 226MF10014
Registrant's Address : Piazzale Luigi Cadorna, 4-20123 MILANO, Italy
Initial Date of Registration : 2014-01-21
Latest Date of Registration : 2014-01-21
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PharmaCompass offers a list of Labetalol 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 Labetalol Hydrochloride manufacturer or Labetalol Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Labetalol Hydrochloride manufacturer or Labetalol Hydrochloride supplier.
PharmaCompass also assists you with knowing the Labetalol Hydrochloride API Price utilized in the formulation of products. Labetalol Hydrochloride API Price is not always fixed or binding as the Labetalol Hydrochloride Price is obtained through a variety of data sources. The Labetalol Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Amipress manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Amipress, including repackagers and relabelers. The FDA regulates Amipress manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Amipress 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 Amipress manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Amipress supplier is an individual or a company that provides Amipress active pharmaceutical ingredient (API) or Amipress finished formulations upon request. The Amipress suppliers may include Amipress 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 Amipress Drug Master File in Japan (Amipress JDMF) empowers Amipress 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 Amipress JDMF during the approval evaluation for pharmaceutical products. At the time of Amipress 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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