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List of Japan Drug Master File (JDMF) for Tox21_300268 Active Pharmaceutical Ingredient submitted to the Review Authority in Japan (PMDA) and listed on PharmaCompass.com

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Flag United Kingdom
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217MF10683
1-2-7 Nishiki, Naka-ku, Nagoya, Aic...
2010-02-12
2005-10-07
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  • TABLET;ORAL - 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL - 20MG **Federal Register notice that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL - 40MG **Federal Register notice that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET, EXTENDED RELEASE;ORAL - 20MG
  • TABLET, EXTENDED RELEASE;ORAL - 40MG
  • TABLET, EXTENDED RELEASE;ORAL - 60MG

Looking for 75330-75-5 / Lovastatin API manufacturers, exporters & distributors?

Lovastatin manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Lovastatin

Synonyms

75330-75-5, Mevinolin, Mevacor, Altoprev, Mevlor, Sivlor

Cas Number

75330-75-5

Unique Ingredient Identifier (UNII)

9LHU78OQFD

About Lovastatin

A fungal metabolite isolated from cultures of Aspergillus terreus. The compound is a potent anticholesteremic agent. It inhibits 3-hydroxy-3-methylglutaryl coenzyme A reductase (HYDROXYMETHYLGLUTARYL COA REDUCTASES), which is the rate-limiting enzyme in cholesterol biosynthesis. It also stimulates the production of low-density lipoprotein receptors in the liver.

Tox21_300268 Manufacturers

A Tox21_300268 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300268, including repackagers and relabelers. The FDA regulates Tox21_300268 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300268 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_300268 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Tox21_300268 Suppliers

A Tox21_300268 supplier is an individual or a company that provides Tox21_300268 active pharmaceutical ingredient (API) or Tox21_300268 finished formulations upon request. The Tox21_300268 suppliers may include Tox21_300268 API manufacturers, exporters, distributors and traders.

click here to find a list of Tox21_300268 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Tox21_300268 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_300268 Drug Master File in Japan (Tox21_300268 JDMF) empowers Tox21_300268 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_300268 JDMF during the approval evaluation for pharmaceutical products. At the time of Tox21_300268 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_300268 suppliers with JDMF on PharmaCompass.

Tox21_300268 Manufacturers | Traders | Suppliers

Tox21_300268 Manufacturers, Traders, Suppliers 1
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We have 1 companies offering Tox21_300268

Get in contact with the supplier of your choice:

  1. Amano Enzyme
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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