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List of Drug Master Files (JDMF) for Tox21_300400 Active Pharmaceutical Ingredient (API) submitted to the Review Authority in Japan (PMDA). Original Data : PMDA Database

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01 Kyongbo Pharmaceutical Co. , Ltd. (1)

02 LUPIN LIMITED. (1)

03 Ohara Pharmaceutical Co., Ltd. (1)

04 Shaoxing Jingxin Pharmaceutical Co. , Ltd. (1)

05 Teva Pharmaceutical Works Private Limited Company (1)

06 Zhejiang Jiangbei Pharmaceutical Co. , Ltd. (1)

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01 SIMVAStatIN-C EXCLUSIVE USE FOR MANUFACTURE (1)

02 Simvastatin (4)

03 Simvastatin "Teva" (1)

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01 China (2)

02 India (1)

03 Israel (1)

04 Japan (1)

05 South Korea (1)

URL Supplier Web Content
220MF10215
174, Sirok-ro, Asan-si, Chungcheong...
2008-10-17
2008-10-17
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303MF10075
Kalpataru Inspire, 3rd Floor, Off W...
2021-05-10
2021-05-10
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217MF11215
121-15 Torino, Koka-cho, Koka-shi, ...
2010-08-26
2005-12-12
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218MF10581
13 Pallagi u(´)t, Debrecen, 4042-H...
2010-07-26
2006-06-22
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228MF10102
Dongdai Village, Zhang'an Street, J...
2021-09-02
2016-05-27
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302MF10018
No. 31, Weisan Road, Hangzhou Bay S...
2022-08-03
2020-01-31
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Looking for 79902-63-9 / Simvastatin API manufacturers, exporters & distributors?

Simvastatin manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Simvastatin

Synonyms

79902-63-9, Zocor, Synvinolin, Mk-733, Sinvacor, Denan

Cas Number

79902-63-9

Unique Ingredient Identifier (UNII)

AGG2FN16EV

About Simvastatin

A derivative of LOVASTATIN and potent competitive inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A reductase (HYDROXYMETHYLGLUTARYL COA REDUCTASES), which is the rate-limiting enzyme in cholesterol biosynthesis. It may also interfere with steroid hormone production. Due to the induction of hepatic LDL RECEPTORS, it increases breakdown of LDL CHOLESTEROL.

Tox21_300400 Manufacturers

A Tox21_300400 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300400, including repackagers and relabelers. The FDA regulates Tox21_300400 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300400 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 Tox21_300400 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Tox21_300400 Suppliers

A Tox21_300400 supplier is an individual or a company that provides Tox21_300400 active pharmaceutical ingredient (API) or Tox21_300400 finished formulations upon request. The Tox21_300400 suppliers may include Tox21_300400 API manufacturers, exporters, distributors and traders.

click here to find a list of Tox21_300400 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Tox21_300400 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 Tox21_300400 Drug Master File in Japan (Tox21_300400 JDMF) empowers Tox21_300400 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 Tox21_300400 JDMF during the approval evaluation for pharmaceutical products. At the time of Tox21_300400 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 Tox21_300400 suppliers with JDMF on PharmaCompass.

Tox21_300400 Manufacturers | Traders | Suppliers

Tox21_300400 Manufacturers, Traders, Suppliers 1
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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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