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
64
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 SS-4219 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SS-4219, including repackagers and relabelers. The FDA regulates SS-4219 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SS-4219 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 SS-4219 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A SS-4219 supplier is an individual or a company that provides SS-4219 active pharmaceutical ingredient (API) or SS-4219 finished formulations upon request. The SS-4219 suppliers may include SS-4219 API manufacturers, exporters, distributors and traders.
click here to find a list of SS-4219 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 SS-4219 Drug Master File in Japan (SS-4219 JDMF) empowers SS-4219 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 SS-4219 JDMF during the approval evaluation for pharmaceutical products. At the time of SS-4219 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 SS-4219 suppliers with JDMF on PharmaCompass.
We have 2 companies offering SS-4219
Get in contact with the supplier of your choice:
