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List of Drug Master Files (JDMF) for DSSTox_CID_29808 Active Pharmaceutical Ingredient (API) submitted to the Review Authority in Japan (PMDA). Original Data : PMDA Database

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01 LUPIN LIMITED. (1)

02 PharmaChem Technologies G. B. Ltd. (1)

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01 Tenofovir Disoproxil Fumarate (1)

02 Tenofovir disoproxil fumarate (1)

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01 Bahamas (1)

02 India (1)

URL Supplier Web Content
229MF10172
Kalpataru Inspire, 3rd Floor, Off W...
2017-08-28
2017-08-28
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URL Supplier Web Content
225MF10169
West Sunrise Highway P. O. Box F-42...
2017-10-03
2013-08-28
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Looking for 202138-50-9 / Tenofovir Disoproxil Fumarate API manufacturers, exporters & distributors?

Tenofovir Disoproxil Fumarate manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Tenofovir Disoproxil Fumarate 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 Tenofovir Disoproxil Fumarate manufacturer or Tenofovir Disoproxil Fumarate supplier for your needs.

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

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

API | Excipient name

Tenofovir Disoproxil Fumarate

Synonyms

202138-50-9, Tenofovir df, Virea, Tenofovir disoproxil fumarate [usan], Pmpa-prodrug, Gs-4331-05

Cas Number

202138-50-9

Unique Ingredient Identifier (UNII)

OTT9J7900I

About Tenofovir Disoproxil Fumarate

An adenine analog REVERSE TRANSCRIPTASE INHIBITOR with antiviral activity against HIV-1 and HEPATITIS B. It is used to treat HIV INFECTIONS and CHRONIC HEPATITIS B, in combination with other ANTIVIRAL AGENTS, due to the emergence of ANTIVIRAL DRUG RESISTANCE when it is used alone.

DSSTox_CID_29808 Manufacturers

A DSSTox_CID_29808 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_CID_29808, including repackagers and relabelers. The FDA regulates DSSTox_CID_29808 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_CID_29808 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_29808 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

DSSTox_CID_29808 Suppliers

A DSSTox_CID_29808 supplier is an individual or a company that provides DSSTox_CID_29808 active pharmaceutical ingredient (API) or DSSTox_CID_29808 finished formulations upon request. The DSSTox_CID_29808 suppliers may include DSSTox_CID_29808 API manufacturers, exporters, distributors and traders.

click here to find a list of DSSTox_CID_29808 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

DSSTox_CID_29808 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_29808 Drug Master File in Japan (DSSTox_CID_29808 JDMF) empowers DSSTox_CID_29808 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_29808 JDMF during the approval evaluation for pharmaceutical products. At the time of DSSTox_CID_29808 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_29808 suppliers with JDMF on PharmaCompass.

DSSTox_CID_29808 Manufacturers | Traders | Suppliers

DSSTox_CID_29808 Manufacturers, Traders, Suppliers 1
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We have 2 companies offering DSSTox_CID_29808

Get in contact with the supplier of your choice:

  1. Lupin Ltd
  2. PharmaChem Technologies
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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