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Looking for 9002-68-0 / Menotropins API manufacturers, exporters & distributors?

Menotropins manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Menotropins

Synonyms

6,6-dimethylheptanal, Menotrophin, 61489-71-2, Schembl1784550, Akos013847259, Gonadotropin from human menopausal urine

Cas Number

9002-68-0

About Menotropins

Extracts of urine from menopausal women that contain high concentrations of pituitary gonadotropins, FOLLICLE STIMULATING HORMONE and LUTEINIZING HORMONE. Menotropins are used to treat infertility. The FSH:LH ratio and degree of purity vary in different preparations.

6,6-Dimethylheptanal Manufacturers

A 6,6-Dimethylheptanal manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 6,6-Dimethylheptanal, including repackagers and relabelers. The FDA regulates 6,6-Dimethylheptanal manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 6,6-Dimethylheptanal API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

6,6-Dimethylheptanal Suppliers

A 6,6-Dimethylheptanal supplier is an individual or a company that provides 6,6-Dimethylheptanal active pharmaceutical ingredient (API) or 6,6-Dimethylheptanal finished formulations upon request. The 6,6-Dimethylheptanal suppliers may include 6,6-Dimethylheptanal API manufacturers, exporters, distributors and traders.

click here to find a list of 6,6-Dimethylheptanal suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

6,6-Dimethylheptanal USDMF

A 6,6-Dimethylheptanal DMF (Drug Master File) is a document detailing the whole manufacturing process of 6,6-Dimethylheptanal active pharmaceutical ingredient (API) in detail. Different forms of 6,6-Dimethylheptanal DMFs exist exist since differing nations have different regulations, such as 6,6-Dimethylheptanal USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A 6,6-Dimethylheptanal DMF submitted to regulatory agencies in the US is known as a USDMF. 6,6-Dimethylheptanal USDMF includes data on 6,6-Dimethylheptanal's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 6,6-Dimethylheptanal USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of 6,6-Dimethylheptanal suppliers with USDMF on PharmaCompass.

6,6-Dimethylheptanal NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing 6,6-Dimethylheptanal as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for 6,6-Dimethylheptanal API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture 6,6-Dimethylheptanal as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain 6,6-Dimethylheptanal and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 6,6-Dimethylheptanal NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of 6,6-Dimethylheptanal suppliers with NDC on PharmaCompass.

6,6-Dimethylheptanal GMP

6,6-Dimethylheptanal 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 6,6-Dimethylheptanal 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 6,6-Dimethylheptanal GMP manufacturer or 6,6-Dimethylheptanal GMP API supplier for your needs.

6,6-Dimethylheptanal CoA

A 6,6-Dimethylheptanal CoA (Certificate of Analysis) is a formal document that attests to 6,6-Dimethylheptanal's compliance with 6,6-Dimethylheptanal specifications and serves as a tool for batch-level quality control.

6,6-Dimethylheptanal CoA mostly includes findings from lab analyses of a specific batch. For each 6,6-Dimethylheptanal 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.

6,6-Dimethylheptanal may be tested according to a variety of international standards, such as European Pharmacopoeia (6,6-Dimethylheptanal EP), 6,6-Dimethylheptanal JP (Japanese Pharmacopeia) and the US Pharmacopoeia (6,6-Dimethylheptanal 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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