Synopsis
Synopsis
0
USDMF
0
CEP/COS
0
EU WC
0
KDMF
0
NDC API
0
VMF
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;dibromide
2. Calcium Bromide [jan]
3. Calcium Bromide, Ultra Dry , 99.978% (metals Basis)
4. Calcium Bromide (jan)
5. Calciumbromid
6. Calcium Bromatum
7. Calcium Bromide Solution
8. Calcium Bromide Anhydrous
9. Hydrobromic Acid Calcium Salt
10. Einecs 232-164-6
11. Brocal (tn)
12. Ca Br2
13. Unii-87cny2eebh
14. Dsstox_cid_24577
15. Dsstox_rid_80326
16. Dsstox_gsid_44577
17. Calcium Bromide,hydrate (9ci)
18. Hsdb 8493
19. Bcp21634
20. Tox21_301859
21. Br1142
22. Akos015902774
23. Ncgc00255890-01
24. Cas-7789-41-5
25. D01723
26. Ec 232-164-6
27. Calcium Bromide, Anhydrous, Beads, -10 Mesh, 99.98% Trace Metals Basis
1. Calcium Dibromide
2. 7789-41-5
3. Calcium Bromide
| Molecular Weight | 199.89 g/mol |
|---|---|
| Molecular Formula | Br2Ca |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 199.79722 g/mol |
| Monoisotopic Mass | 197.79927 g/mol |
| Topological Polar Surface Area | 0 Ų |
| Heavy Atom Count | 3 |
| Formal Charge | 0 |
| Complexity | 2.8 |
| 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 |
Market Place
ABOUT THIS PAGE
A Calcium Bromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Calcium Bromide, including repackagers and relabelers. The FDA regulates Calcium Bromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Calcium Bromide 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 Calcium Bromide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Calcium Bromide supplier is an individual or a company that provides Calcium Bromide active pharmaceutical ingredient (API) or Calcium Bromide finished formulations upon request. The Calcium Bromide suppliers may include Calcium Bromide API manufacturers, exporters, distributors and traders.
click here to find a list of Calcium Bromide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Calcium Bromide Drug Master File in Japan (Calcium Bromide JDMF) empowers Calcium Bromide API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Calcium Bromide JDMF during the approval evaluation for pharmaceutical products. At the time of Calcium Bromide JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Calcium Bromide suppliers with JDMF on PharmaCompass.
Calcium Bromide 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 Calcium Bromide 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 Calcium Bromide GMP manufacturer or Calcium Bromide GMP API supplier for your needs.
A Calcium Bromide CoA (Certificate of Analysis) is a formal document that attests to Calcium Bromide's compliance with Calcium Bromide specifications and serves as a tool for batch-level quality control.
Calcium Bromide CoA mostly includes findings from lab analyses of a specific batch. For each Calcium Bromide 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.
Calcium Bromide may be tested according to a variety of international standards, such as European Pharmacopoeia (Calcium Bromide EP), Calcium Bromide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Calcium Bromide USP).
LOOKING FOR A SUPPLIER?
