Synopsis
Synopsis
0
API Suppliers
0
USDMF
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
Listed Suppliers
0
API
0
FDF
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
EDQM
0
USP
0
JP
0
Others
0
US Patents
0
US Exclusivities
0
Health Canada Patents
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
1. Calcium Beta-hydroxy-beta-methylbutyrate
2. Hmb-ca:calcium
3. A-hydroxy-
4. A-methyl Butyrate
5. Bcp16075
6. Calcium 3-hydroxy-3-methyl Butyrate
7. 236c725
| Molecular Weight | 274.32 g/mol |
|---|---|
| Molecular Formula | C10H18CaO6 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 6 |
| Exact Mass | 274.0729291 g/mol |
| Monoisotopic Mass | 274.0729291 g/mol |
| Topological Polar Surface Area | 121 Ų |
| Heavy Atom Count | 17 |
| Formal Charge | 0 |
| Complexity | 223 |
| 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 | 3 |
ABOUT THIS PAGE
A 236C725 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 236C725, including repackagers and relabelers. The FDA regulates 236C725 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 236C725 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 236C725 supplier is an individual or a company that provides 236C725 active pharmaceutical ingredient (API) or 236C725 finished formulations upon request. The 236C725 suppliers may include 236C725 API manufacturers, exporters, distributors and traders.
236C725 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 236C725 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 236C725 GMP manufacturer or 236C725 GMP API supplier for your needs.
A 236C725 CoA (Certificate of Analysis) is a formal document that attests to 236C725's compliance with 236C725 specifications and serves as a tool for batch-level quality control.
236C725 CoA mostly includes findings from lab analyses of a specific batch. For each 236C725 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.
236C725 may be tested according to a variety of international standards, such as European Pharmacopoeia (236C725 EP), 236C725 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (236C725 USP).
LOOKING FOR A SUPPLIER?
