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List of Drug Master Files (JDMF) for DSSTox_CID_3692 Active Pharmaceutical Ingredient (API) submitted to the Review Authority in Japan (PMDA). Original Data : PMDA Database

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01 CHUNGHWA CHEMICAL SYNTHESIS & BIOTECH CO. , LTD. (1)

02 Chunghwa Chemical Synthesis & Biotech Co. , Ltd. (1)

03 Ohara Pharmaceutical Co., Ltd. (1)

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01 Trandolapril (3)

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01 Japan (1)

02 Taiwan (2)

URL Supplier Web Content
225MF10083
No. 1, Tung-Hsing St. , Shu-Lin, Ne...
2020-03-23
2013-04-23
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218MF10666
1, Tung-Hsing, Street, Shu-Lin 238,...
2006-07-24
2006-07-24
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217MF11216
121-15 Torino, Koka-cho, Koka-shi, ...
2006-12-01
2005-12-12
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Looking for 87679-37-6 / Trandolapril API manufacturers, exporters & distributors?

Trandolapril manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Trandolapril 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 Trandolapril manufacturer or Trandolapril supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Trandolapril manufacturer or Trandolapril supplier.

PharmaCompass also assists you with knowing the Trandolapril API Price utilized in the formulation of products. Trandolapril API Price is not always fixed or binding as the Trandolapril Price is obtained through a variety of data sources. The Trandolapril Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Trandolapril

Synonyms

87679-37-6, Mavik, Gopten, Odrik, Trandolaprilum [latin], Ru-44570

Cas Number

87679-37-6

Unique Ingredient Identifier (UNII)

1T0N3G9CRC

About Trandolapril

Trandolapril is a non-sulfhydryl angiotensin-converting enzyme (ACE) inhibitor with antihypertensive activity. As a prodrug, trandolapril is converted by de-esterification in the liver into its active form trandolaprilat. Trandolaprilat competitively binds to and inhibits ACE, thereby blocking the conversion of angiotensin I to angiotensin II. This prevents the potent vasoconstrictive actions of angiotensin II and results in vasodilation. Trandolaprilat also decreases angiotensin II-induced aldosterone secretion by the adrenal cortex, which leads to an increase in sodium excretion and subsequently increases water outflow.

DSSTox_CID_3692 Manufacturers

A DSSTox_CID_3692 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_CID_3692, including repackagers and relabelers. The FDA regulates DSSTox_CID_3692 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_CID_3692 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 DSSTox_CID_3692 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

DSSTox_CID_3692 Suppliers

A DSSTox_CID_3692 supplier is an individual or a company that provides DSSTox_CID_3692 active pharmaceutical ingredient (API) or DSSTox_CID_3692 finished formulations upon request. The DSSTox_CID_3692 suppliers may include DSSTox_CID_3692 API manufacturers, exporters, distributors and traders.

click here to find a list of DSSTox_CID_3692 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

DSSTox_CID_3692 JDMF

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 DSSTox_CID_3692 Drug Master File in Japan (DSSTox_CID_3692 JDMF) empowers DSSTox_CID_3692 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 DSSTox_CID_3692 JDMF during the approval evaluation for pharmaceutical products. At the time of DSSTox_CID_3692 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 DSSTox_CID_3692 suppliers with JDMF on PharmaCompass.

DSSTox_CID_3692 Manufacturers | Traders | Suppliers

DSSTox_CID_3692 Manufacturers, Traders, Suppliers 1
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We have 2 companies offering DSSTox_CID_3692

Get in contact with the supplier of your choice:

  1. Chunghwa Chemical Synthesis & Biotech
  2. Ohara Pharmaceutical
Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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