TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1Teva API India Private Limited
02 1Olon S. p. A.
01 1Amitriptyline Hydrochloride "Teva / Malanpur"
02 1Amitriptyline hydrochloride
01 1Israel
02 1Italy
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Amitriptyline hydrochloride "Teva/Malanpur"
Registration Number : 302MF10137
Registrant's Address : Plot No. 2G, 2H, 2I, Udyog Vihar, Greater Noida-201 308 (U.P.) India
Initial Date of Registration : 2020-11-26
Latest Date of Registration : 2020-11-26
Registration Number : 222MF10063
Registrant's Address : Strada Rivoltana Km 6/7 20053 Rodano Milano Italy
Initial Date of Registration : 2010-02-22
Latest Date of Registration : 2010-02-22
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PharmaCompass offers a list of Amitriptyline 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 Amitriptyline Hydrochloride manufacturer or Amitriptyline Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Amitriptyline Hydrochloride manufacturer or Amitriptyline Hydrochloride supplier.
PharmaCompass also assists you with knowing the Amitriptyline Hydrochloride API Price utilized in the formulation of products. Amitriptyline Hydrochloride API Price is not always fixed or binding as the Amitriptyline Hydrochloride Price is obtained through a variety of data sources. The Amitriptyline Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A LIMBITROL DS manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LIMBITROL DS, including repackagers and relabelers. The FDA regulates LIMBITROL DS manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LIMBITROL DS 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 LIMBITROL DS manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A LIMBITROL DS supplier is an individual or a company that provides LIMBITROL DS active pharmaceutical ingredient (API) or LIMBITROL DS finished formulations upon request. The LIMBITROL DS suppliers may include LIMBITROL DS API manufacturers, exporters, distributors and traders.
click here to find a list of LIMBITROL DS 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 LIMBITROL DS Drug Master File in Japan (LIMBITROL DS JDMF) empowers LIMBITROL DS 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 LIMBITROL DS JDMF during the approval evaluation for pharmaceutical products. At the time of LIMBITROL DS 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 LIMBITROL DS suppliers with JDMF on PharmaCompass.
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