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| Molecular Weight | 275.24 g/mol |
|---|---|
| Molecular Formula | C10H14N5NaO3 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 5 |
| Exact Mass | 275.09943361 g/mol |
| Monoisotopic Mass | 275.09943361 g/mol |
| Topological Polar Surface Area | 129 A^2 |
| Heavy Atom Count | 19 |
| Formal Charge | 0 |
| Complexity | 354 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
Global Sales Information
US Medicaid Prescriptions
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]ABOUT THIS PAGE
A Penciclovir Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Penciclovir Sodium, including repackagers and relabelers. The FDA regulates Penciclovir Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Penciclovir Sodium 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 Penciclovir Sodium supplier is an individual or a company that provides Penciclovir Sodium active pharmaceutical ingredient (API) or Penciclovir Sodium finished formulations upon request. The Penciclovir Sodium suppliers may include Penciclovir Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Penciclovir Sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Penciclovir Sodium DMF (Drug Master File) is a document detailing the whole manufacturing process of Penciclovir Sodium active pharmaceutical ingredient (API) in detail. Different forms of Penciclovir Sodium DMFs exist exist since differing nations have different regulations, such as Penciclovir Sodium USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Penciclovir Sodium DMF submitted to regulatory agencies in the US is known as a USDMF. Penciclovir Sodium USDMF includes data on Penciclovir Sodium's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Penciclovir Sodium USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Penciclovir Sodium suppliers with USDMF on PharmaCompass.
Penciclovir Sodium 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 Penciclovir Sodium 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 Penciclovir Sodium GMP manufacturer or Penciclovir Sodium GMP API supplier for your needs.
A Penciclovir Sodium CoA (Certificate of Analysis) is a formal document that attests to Penciclovir Sodium's compliance with Penciclovir Sodium specifications and serves as a tool for batch-level quality control.
Penciclovir Sodium CoA mostly includes findings from lab analyses of a specific batch. For each Penciclovir Sodium 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.
Penciclovir Sodium may be tested according to a variety of international standards, such as European Pharmacopoeia (Penciclovir Sodium EP), Penciclovir Sodium JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Penciclovir Sodium USP).
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