01 1ARAGEN LIFE SCIENCES LIMITED.
02 1JUBILANT BIOSYS LIMITED.
03 1Proto Chemicals AG
04 1SUN PHARMACEUTICAL INDUSTRIES LIMITED.
05 1Saneca Pharmaceuticals a. s.
06 1Tateyama Chemical Co., Ltd.
07 1Zydus Cadila Healthcare Ltd.
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PharmaCompass offers a list of Tramadol 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 Tramadol Hydrochloride manufacturer or Tramadol Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tramadol Hydrochloride manufacturer or Tramadol Hydrochloride supplier.
PharmaCompass also assists you with knowing the Tramadol Hydrochloride API Price utilized in the formulation of products. Tramadol Hydrochloride API Price is not always fixed or binding as the Tramadol Hydrochloride Price is obtained through a variety of data sources. The Tramadol Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ultram ER manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ultram ER, including repackagers and relabelers. The FDA regulates Ultram ER manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ultram ER 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 Ultram ER manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ultram ER supplier is an individual or a company that provides Ultram ER active pharmaceutical ingredient (API) or Ultram ER finished formulations upon request. The Ultram ER suppliers may include Ultram ER API manufacturers, exporters, distributors and traders.
click here to find a list of Ultram ER 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 Ultram ER Drug Master File in Japan (Ultram ER JDMF) empowers Ultram ER 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 Ultram ER JDMF during the approval evaluation for pharmaceutical products. At the time of Ultram ER 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 Ultram ER suppliers with JDMF on PharmaCompass.
We have 7 companies offering Ultram ER
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