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1. 1262751-08-5
2. Ova Peptide (257-264) (tfa)
3. (2s)-2-[[(2s)-6-amino-2-[[(2s)-2-[[(2s)-2-[[(2s)-4-amino-2-[[(2s,3s)-2-[[(2s,3s)-2-[[(2s)-2-amino-3-hydroxypropanoyl]amino]-3-methylpentanoyl]amino]-3-methylpentanoyl]amino]-4-oxobutanoyl]amino]-3-phenylpropanoyl]amino]-4-carboxybutanoyl]amino]hexanoyl]amino]-4-methylpentanoic Acid;2,2,2-trifluoroacetic Acid
4. Hy-p1489a
5. Ova Peptide 257-264 Tfa
6. Cs-0089371
7. Ovalbumin (257-264) Chicken, >=97% (hplc)
| Molecular Weight | 1077.2 g/mol |
|---|---|
| Molecular Formula | C47H75F3N10O15 |
| Hydrogen Bond Donor Count | 14 |
| Hydrogen Bond Acceptor Count | 20 |
| Rotatable Bond Count | 33 |
| Exact Mass | 1076.53654621 g/mol |
| Monoisotopic Mass | 1076.53654621 g/mol |
| Topological Polar Surface Area | 431 Ų |
| Heavy Atom Count | 75 |
| Formal Charge | 0 |
| Complexity | 1780 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 10 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
REF. STANDARDS & IMPURITIES
ANALYTICAL
Analytical Methods
ABOUT THIS PAGE
A pOV8 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of pOV8, including repackagers and relabelers. The FDA regulates pOV8 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. pOV8 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A pOV8 supplier is an individual or a company that provides pOV8 active pharmaceutical ingredient (API) or pOV8 finished formulations upon request. The pOV8 suppliers may include pOV8 API manufacturers, exporters, distributors and traders.
pOV8 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 pOV8 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 pOV8 GMP manufacturer or pOV8 GMP API supplier for your needs.
A pOV8 CoA (Certificate of Analysis) is a formal document that attests to pOV8's compliance with pOV8 specifications and serves as a tool for batch-level quality control.
pOV8 CoA mostly includes findings from lab analyses of a specific batch. For each pOV8 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.
pOV8 may be tested according to a variety of international standards, such as European Pharmacopoeia (pOV8 EP), pOV8 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (pOV8 USP).
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