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1. Grf(1-43)-oh
2. Growth Hormone Releasing Factor 43
3. Hpgrf(1-43)oh
4. Rat Growth Hormone-releasing Factor(1-43)
5. Rgrf 43
6. Rgrf(1-43)-oh
7. Rgrf(1-43)oh
8. Rhgrf(1-43)
9. Somaotropin Releasing Hormone (1-43)oh
10. Somatotropin Releasing Factor 43
1. 86472-71-1
2. Rgrf 43
3. Hpgrf(1-43)oh
4. Rhgrf(1-43)
5. Rgrf(1-43)-oh
6. Grf(1-43)-oh
7. Somatotropin Releasing Factor 43
8. Growth Hormone Releasing Factor 43
9. Somatropin Recombinant
10. Somaotropin Releasing Hormone (1-43)oh
11. Rat Growth Hormone-releasing Factor(1-43)
12. Dtxsid30235580
13. Somatoliberin (human Pancreatic Islet), 1-l-histidine-8-l-serine -12-l-arginine-13-l-isoleucine-18-l-tyrosine-24-l-histidine-25-l-glutamic Acid-28-l-asparagine-34-l-arginine-38-l-glutamine-39-l-arginine-40-l-serine-42-l-phenylalanine-43-l-asparagine-44-de-l-leucinamide-
| Molecular Weight | 5234 g/mol |
|---|---|
| Molecular Formula | C225H360N76O67S |
| XLogP3 | -23.5 |
| Hydrogen Bond Donor Count | 86 |
| Hydrogen Bond Acceptor Count | 79 |
| Rotatable Bond Count | 189 |
| Exact Mass | 5232.6886961 g/mol |
| Monoisotopic Mass | 5230.6819865 g/mol |
| Topological Polar Surface Area | 2440 Ų |
| Heavy Atom Count | 369 |
| Formal Charge | 0 |
| Complexity | 13100 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 45 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |

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PharmaCompass offers a list of Somatropin 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 Somatropin manufacturer or Somatropin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Somatropin manufacturer or Somatropin supplier.
PharmaCompass also assists you with knowing the Somatropin API Price utilized in the formulation of products. Somatropin API Price is not always fixed or binding as the Somatropin Price is obtained through a variety of data sources. The Somatropin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Somatropin recombinant manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Somatropin recombinant, including repackagers and relabelers. The FDA regulates Somatropin recombinant manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Somatropin recombinant 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 Somatropin recombinant manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Somatropin recombinant supplier is an individual or a company that provides Somatropin recombinant active pharmaceutical ingredient (API) or Somatropin recombinant finished formulations upon request. The Somatropin recombinant suppliers may include Somatropin recombinant API manufacturers, exporters, distributors and traders.
click here to find a list of Somatropin recombinant suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Somatropin recombinant DMF (Drug Master File) is a document detailing the whole manufacturing process of Somatropin recombinant active pharmaceutical ingredient (API) in detail. Different forms of Somatropin recombinant DMFs exist exist since differing nations have different regulations, such as Somatropin recombinant USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Somatropin recombinant DMF submitted to regulatory agencies in the US is known as a USDMF. Somatropin recombinant USDMF includes data on Somatropin recombinant's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Somatropin recombinant USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Somatropin recombinant suppliers with USDMF on PharmaCompass.
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 Somatropin recombinant as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Somatropin recombinant API and other APIs are published in this directory by the FDA.
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 Somatropin recombinant 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.
The NDC directory also contains data on finished compounded human drug products that contain Somatropin recombinant and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Somatropin recombinant NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Somatropin recombinant suppliers with NDC on PharmaCompass.
Somatropin recombinant 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 Somatropin recombinant 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 Somatropin recombinant GMP manufacturer or Somatropin recombinant GMP API supplier for your needs.
A Somatropin recombinant CoA (Certificate of Analysis) is a formal document that attests to Somatropin recombinant's compliance with Somatropin recombinant specifications and serves as a tool for batch-level quality control.
Somatropin recombinant CoA mostly includes findings from lab analyses of a specific batch. For each Somatropin recombinant 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.
Somatropin recombinant may be tested according to a variety of international standards, such as European Pharmacopoeia (Somatropin recombinant EP), Somatropin recombinant JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Somatropin recombinant USP).