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Looking for 180916-16-9 / Lasofoxifene API manufacturers, exporters & distributors?

Lasofoxifene manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Lasofoxifene

Synonyms

180916-16-9, Rac-lasofoxifene, Oporia, Cp 336156, 180915-78-0, (5r,6s)-6-phenyl-5-[4-(2-pyrrolidin-1-ylethoxy)phenyl]-5,6,7,8-tetrahydronaphthalen-2-ol

Cas Number

180916-16-9

Unique Ingredient Identifier (UNII)

337G83N988

About Lasofoxifene

Lasofoxifene is a non-steroidal, naphthalene-derived, third-generation selective estrogen receptor modulator (SERM) with potential antineoplastic and anti-osteoporotic activities. Upon oral administration, lasofoxifene selectively binds to both estrogen receptor alpha (ERalpha; ESR1) and estrogen receptor beta (ERbeta; ESR2) with high affinity and mimics the effects of endogenous estradiol with varying agonist and antagonist effects in ER-expressing tissues. Blockade of ERalpha by lasofoxifene may potentially inhibit estrogen-dependent cancer cell proliferation in ER-expressing cancers. Lasofoxifene may also bind to the certain mutant forms of ERalpha, including the Y537S ESR1 mutant, making it potentially useful in the treatment of tumors that have acquired resistance to other ER-targeting agents.

Lasofoxifene Manufacturers

A Lasofoxifene manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lasofoxifene, including repackagers and relabelers. The FDA regulates Lasofoxifene manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lasofoxifene API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

Lasofoxifene Suppliers

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

Lasofoxifene GMP

Lasofoxifene Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.

GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).

PharmaCompass offers a list of Lasofoxifene GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Lasofoxifene GMP manufacturer or Lasofoxifene GMP API supplier for your needs.

Lasofoxifene CoA

A Lasofoxifene CoA (Certificate of Analysis) is a formal document that attests to Lasofoxifene's compliance with Lasofoxifene specifications and serves as a tool for batch-level quality control.

Lasofoxifene CoA mostly includes findings from lab analyses of a specific batch. For each Lasofoxifene CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.

Lasofoxifene may be tested according to a variety of international standards, such as European Pharmacopoeia (Lasofoxifene EP), Lasofoxifene JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Lasofoxifene USP).

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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