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

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01 Ajinomoto Co., Inc. (2)

02 DIVI'S LABORATORIES LIMITED (1)

03 Shandong Xinhua Pharmaceutical Co. , Ltd. (1)

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01 Japanese Pharmacopoeia levodopa (production only) (2)

02 L-Dihydroxyphenylalanine (1)

03 Levodopa (1)

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01 China (1)

02 India (1)

03 Japan (2)

URL Supplier Web Content
302MF10140
1-15-1 Kyobashi, Chuo-ku, Tokyo
2020-11-26
2020-11-26
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URL Supplier Web Content
221MF10284
1-15-1 Kyobashi, Chuo-ku, Tokyo
2009-12-22
2009-12-22
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URL Supplier Web Content
227MF10235
1-72/23(P)/DIVIS/303, Divi Towers, ...
2018-04-12
2015-09-24
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URL Supplier Web Content
221MF10029
No. 1, Lutai Road, High-tech Distri...
2009-02-09
2009-02-09
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Looking for 59-92-7 / Etilevodopa API manufacturers, exporters & distributors?

Etilevodopa manufacturers, exporters & distributors 1

62

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

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

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

API | Excipient name

Etilevodopa

Synonyms

L-dopa, 59-92-7, Dopar, 3,4-dihydroxy-l-phenylalanine, 3-hydroxy-l-tyrosine, Bendopa

Cas Number

59-92-7

Unique Ingredient Identifier (UNII)

46627O600J

About Etilevodopa

The naturally occurring form of DIHYDROXYPHENYLALANINE and the immediate precursor of DOPAMINE. Unlike dopamine itself, it can be taken orally and crosses the blood-brain barrier. It is rapidly taken up by dopaminergic neurons and converted to DOPAMINE. It is used for the treatment of PARKINSONIAN DISORDERS and is usually given with agents that inhibit its conversion to dopamine outside of the central nervous system.

Etilevodopa Manufacturers

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

Etilevodopa Suppliers

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

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

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

Etilevodopa Manufacturers | Traders | Suppliers

Etilevodopa Manufacturers, Traders, Suppliers 1
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We have 3 companies offering Etilevodopa

Get in contact with the supplier of your choice:

  1. Ajinomoto Company
  2. Divis Laboratories
  3. Shandong Xinhua 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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