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1. 5-ala
| Molecular Weight | 167.59 g/mol |
|---|---|
| Molecular Formula | C5H10ClNO3 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 4 |
| Exact Mass | 167.0349209 g/mol |
| Monoisotopic Mass | 167.0349209 g/mol |
| Topological Polar Surface Area | 82 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 121 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
ABOUT THIS PAGE
A Delta-Aminolevulinic Acid HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Delta-Aminolevulinic Acid HCl, including repackagers and relabelers. The FDA regulates Delta-Aminolevulinic Acid HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Delta-Aminolevulinic Acid HCl 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 Delta-Aminolevulinic Acid HCl supplier is an individual or a company that provides Delta-Aminolevulinic Acid HCl active pharmaceutical ingredient (API) or Delta-Aminolevulinic Acid HCl finished formulations upon request. The Delta-Aminolevulinic Acid HCl suppliers may include Delta-Aminolevulinic Acid HCl API manufacturers, exporters, distributors and traders.
click here to find a list of Delta-Aminolevulinic Acid HCl suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Delta-Aminolevulinic Acid HCl DMF (Drug Master File) is a document detailing the whole manufacturing process of Delta-Aminolevulinic Acid HCl active pharmaceutical ingredient (API) in detail. Different forms of Delta-Aminolevulinic Acid HCl DMFs exist exist since differing nations have different regulations, such as Delta-Aminolevulinic Acid HCl USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Delta-Aminolevulinic Acid HCl DMF submitted to regulatory agencies in the US is known as a USDMF. Delta-Aminolevulinic Acid HCl USDMF includes data on Delta-Aminolevulinic Acid HCl's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Delta-Aminolevulinic Acid HCl USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Delta-Aminolevulinic Acid HCl suppliers with USDMF on PharmaCompass.
Delta-Aminolevulinic Acid HCl 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 Delta-Aminolevulinic Acid HCl 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 Delta-Aminolevulinic Acid HCl GMP manufacturer or Delta-Aminolevulinic Acid HCl GMP API supplier for your needs.
A Delta-Aminolevulinic Acid HCl CoA (Certificate of Analysis) is a formal document that attests to Delta-Aminolevulinic Acid HCl's compliance with Delta-Aminolevulinic Acid HCl specifications and serves as a tool for batch-level quality control.
Delta-Aminolevulinic Acid HCl CoA mostly includes findings from lab analyses of a specific batch. For each Delta-Aminolevulinic Acid HCl 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.
Delta-Aminolevulinic Acid HCl may be tested according to a variety of international standards, such as European Pharmacopoeia (Delta-Aminolevulinic Acid HCl EP), Delta-Aminolevulinic Acid HCl JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Delta-Aminolevulinic Acid HCl USP).
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