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1. 111in Radioisotope
2. In-111 Radioisotope
1. Indium In-111
2. 111in
3. Indium, Isotope Of Mass 111
4. Indium (111 In)
5. 15750-15-9
6. E9ngc49e0t
7. Unii-e9ngc49e0t
8. 111in Radioisotope
9. In-111 Radioisotope
10. Indium In 111
11. Indium (111in)
12. Indium, In-111
13. Isotope Of Mass 111
14. Indium In 111 [vandf]
15. Dtxsid001019286
16. Db11916
17. Indium (111 In) [who-dd]
18. Q6025171
19. 454695-43-3
| Molecular Weight | 110.90511 g/mol |
|---|---|
| Molecular Formula | In |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 0 |
| Exact Mass | 110.90511 g/mol |
| Monoisotopic Mass | 110.90511 g/mol |
| Topological Polar Surface Area | 0 Ų |
| Heavy Atom Count | 1 |
| Formal Charge | 0 |
| Complexity | 0 |
| Isotope Atom Count | 1 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
FDF Dossiers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Europe
Regulatory Info :
Registration Country : Sweden
Brand Name : Indium (In-111), oxine GE Healthcare
Dosage Form : RADIOPHARMACEUTICAL DRUGS
Dosage Strength : 37 MBQ / ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Indium (In-111) oxinate Mallinckrodt Medical
Dosage Form : RADIOPHARMACEUTICAL DRUGS
Dosage Strength : 37 MBQ / ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Digital Content
NEWS #PharmaBuzz
ABOUT THIS PAGE
A INDIUM 111 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of INDIUM 111, including repackagers and relabelers. The FDA regulates INDIUM 111 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. INDIUM 111 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 INDIUM 111 supplier is an individual or a company that provides INDIUM 111 active pharmaceutical ingredient (API) or INDIUM 111 finished formulations upon request. The INDIUM 111 suppliers may include INDIUM 111 API manufacturers, exporters, distributors and traders.
click here to find a list of INDIUM 111 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A INDIUM 111 DMF (Drug Master File) is a document detailing the whole manufacturing process of INDIUM 111 active pharmaceutical ingredient (API) in detail. Different forms of INDIUM 111 DMFs exist exist since differing nations have different regulations, such as INDIUM 111 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A INDIUM 111 DMF submitted to regulatory agencies in the US is known as a USDMF. INDIUM 111 USDMF includes data on INDIUM 111's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The INDIUM 111 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of INDIUM 111 suppliers with USDMF on PharmaCompass.
INDIUM 111 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 INDIUM 111 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 INDIUM 111 GMP manufacturer or INDIUM 111 GMP API supplier for your needs.
A INDIUM 111 CoA (Certificate of Analysis) is a formal document that attests to INDIUM 111's compliance with INDIUM 111 specifications and serves as a tool for batch-level quality control.
INDIUM 111 CoA mostly includes findings from lab analyses of a specific batch. For each INDIUM 111 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.
INDIUM 111 may be tested according to a variety of international standards, such as European Pharmacopoeia (INDIUM 111 EP), INDIUM 111 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (INDIUM 111 USP).
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