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List of Drug Master Files (JDMF) for MolPort-002-042-265 Active Pharmaceutical Ingredient (API) submitted to the Review Authority in Japan (PMDA). Original Data : PMDA Database

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01 Ace Japan Co., Ltd. (1)

02 MEDICHEM, S. A. (1)

03 SCI Pharmtech, Inc. (1)

04 Sumitomo Chemical Co., Ltd. (1)

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01 Japanese Pharmacopoeia Probucol (1)

02 Japanese Pharmacopoeia probucol (1)

03 Probucol (2)

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01 Gabon (1)

02 Japan (2)

03 Taiwan (1)

URL Supplier Web Content
305MF10113
5850-1 Higashineko, Higashine City,...
2023-10-04
2023-10-04
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URL Supplier Web Content
229MF10022
No. 61, Ln. 309, Haihu N. Rd. , Luz...
2017-01-31
2017-01-31
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URL Supplier Web Content
222MF10231
2-27-1 Shinkawa, Chuo-ku, Tokyo
2010-09-24
2010-09-24
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MEDICHEM, S. A.

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Virtual Booth Virtual Booth
Digital Content Digital Content
URL Supplier Web Content
221MF10181
6-8, Fructo(´)s Gelabert 08970 San...
2009-08-07
2009-08-07
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Looking for 23288-49-5 / Probucol API manufacturers, exporters & distributors?

Probucol manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Probucol

Synonyms

23288-49-5, Lorelco, Biphenabid, Bisphenabid, Lurselle, Bisbid

Cas Number

23288-49-5

Unique Ingredient Identifier (UNII)

P3CTH044XJ

About Probucol

A drug used to lower LDL and HDL cholesterol yet has little effect on serum-triglyceride or VLDL cholesterol. (From Martindale, The Extra Pharmacopoeia, 30th ed, p993).

MolPort-002-042-265 Manufacturers

A MolPort-002-042-265 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-002-042-265, including repackagers and relabelers. The FDA regulates MolPort-002-042-265 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-002-042-265 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 MolPort-002-042-265 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

MolPort-002-042-265 Suppliers

A MolPort-002-042-265 supplier is an individual or a company that provides MolPort-002-042-265 active pharmaceutical ingredient (API) or MolPort-002-042-265 finished formulations upon request. The MolPort-002-042-265 suppliers may include MolPort-002-042-265 API manufacturers, exporters, distributors and traders.

click here to find a list of MolPort-002-042-265 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

MolPort-002-042-265 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 MolPort-002-042-265 Drug Master File in Japan (MolPort-002-042-265 JDMF) empowers MolPort-002-042-265 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 MolPort-002-042-265 JDMF during the approval evaluation for pharmaceutical products. At the time of MolPort-002-042-265 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 MolPort-002-042-265 suppliers with JDMF on PharmaCompass.

MolPort-002-042-265 Manufacturers | Traders | Suppliers

MolPort-002-042-265 Manufacturers, Traders, Suppliers 1
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We have 3 companies offering MolPort-002-042-265

Get in contact with the supplier of your choice:

  1. ACE Japan Co Ltd
  2. SCI PHARMTECH
  3. Sumitomo Chemical
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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