Synopsis
Synopsis
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USDMF
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CEP/COS
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JDMF
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EU WC
0
KDMF
0
NDC API
0
VMF
0
FDA Orange Book
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Europe
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South Africa
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Listed Dossiers
DRUG PRODUCT COMPOSITIONS
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US Patents
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US Exclusivities
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Health Canada Patents
US Medicaid
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Annual Reports
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Regulatory FDF Prices
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API
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FDF
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Data Compilation #PharmaFlow
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Stock Recap #PipelineProspector
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| Molecular Weight | 627.8 g/mol |
|---|---|
| Molecular Formula | C38H49N3O5 |
| XLogP3 | 8.8 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 16 |
| Exact Mass | 627.36722167 g/mol |
| Monoisotopic Mass | 627.36722167 g/mol |
| Topological Polar Surface Area | 98.2 A^2 |
| Heavy Atom Count | 46 |
| Formal Charge | 0 |
| Complexity | 1290 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 2 |
| Defined Bond Stereocenter Count | 2 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
Related Excipient Companies
Excipients by Applications
Dosage Form : Cream / Lotion / Ointment, Injectable / Parenteral
Grade : Topical, Parenteral
Category : Parenteral, Topical
Dosage Form : Emulsion
Grade : Topical
Category : Emulsifying Agents, Surfactant & Foaming Agents, Topical
Dosage Form : Cream / Lotion / Ointment, Gel, Injectable / Parenteral, Softgel Capsule, Softgels
Grade : Parenteral, Topical, Oral
Category : Fillers, Diluents & Binders, Film Formers & Plasticizers, Parenteral, Surfactant & Foaming Agents, Thickeners and Stabilizers, Topical
Brand Name : Polyethylene Glycol 400
Application : Fillers, Diluents & Binders, Film Formers & Plasticizers, Parenteral, Surfactant & Foaming Agents, Thickeners and Stabilizers, Topical
Excipient Details : PEG 400 is used as a suspending agent, stabilizer, plasticizer and filler in OSDs, liquids & semi-solids and as a solvent for parenteral formulations.
Dosage Form : Cream / Lotion / Ointment, Emulsion, Injectable / Parenteral, Softgels, Tablet
Grade : Oral, Topical, Parenteral
Category : Film Formers & Plasticizers, Parenteral, Topical

Dosage Form : Cream / Lotion / Ointment, Gel, Injectable / Parenteral, Softgels
Grade : Parenteral, Oral, Topical
Category : Film Formers & Plasticizers, Parenteral, Thickeners and Stabilizers, Topical
Dosage Form : Injectable / Parenteral, Solution
Grade : Parenteral
Category : Controlled & Modified Release, Parenteral
Application : Controlled & Modified Release, Parenteral
Excipient Details : Cholesterol is used as a sustained release material for drug delivery systems in injectable formulations.
Dosage Form : Cream / Lotion / Ointment, Emulsion, Injectable / Parenteral
Grade : Topical, Parenteral
Category : Emulsifying Agents, Parenteral, Solubilizers, Surfactant & Foaming Agents, Topical
Dosage Form : Capsule, Cream / Lotion / Ointment, Tablet
Grade : Not Available
Category : Controlled & Modified Release, Solubilizers, Thickeners and Stabilizers, Topical
Brand Name : Glyceryl Monostearate
Application : Controlled & Modified Release, Solubilizers, Thickeners and Stabilizers, Topical
Excipient Details : Glyceryl monostearate is used as an emollient, solubilizer, stabilizer, emulsifier, and sustained-release agent in tablets and capsules.
Pharmacopoeia Ref : Not Available
Technical Specs : Not Available
Ingredient(s) : Glyceryl Monostearate
Dosage Form : Capsule, Cream / Lotion / Ointment
Grade : Topical and Oral
Category : Film Formers & Plasticizers, Topical
Application : Film Formers & Plasticizers, Topical
Excipients Web Link
Dosage Form : Cream / Lotion / Ointment, Gel, Solution
Grade : Oral, Topical
Category : Emulsifying Agents, Solubilizers, Topical
Application : Emulsifying Agents, Solubilizers, Topical
Excipient Details : Hydrosol 50 is used as a solubilizer and emulsifying agent in oral and topical liquid and semi-solid dosage forms.
Pharmacopoeia Ref : USP/NF
Technical Specs : N/A
Ingredient(s) : Polyoxyl 40 Hydrogenated Castor Oil
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
37
PharmaCompass offers a list of Bemotrizinol API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Bemotrizinol manufacturer or Bemotrizinol supplier for your needs.
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A Bemotrizinol (USAN/INN) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bemotrizinol (USAN/INN), including repackagers and relabelers. The FDA regulates Bemotrizinol (USAN/INN) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bemotrizinol (USAN/INN) API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Bemotrizinol (USAN/INN) supplier is an individual or a company that provides Bemotrizinol (USAN/INN) active pharmaceutical ingredient (API) or Bemotrizinol (USAN/INN) finished formulations upon request. The Bemotrizinol (USAN/INN) suppliers may include Bemotrizinol (USAN/INN) API manufacturers, exporters, distributors and traders.
click here to find a list of Bemotrizinol (USAN/INN) suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
Bemotrizinol (USAN/INN) 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 Bemotrizinol (USAN/INN) GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Bemotrizinol (USAN/INN) GMP manufacturer or Bemotrizinol (USAN/INN) GMP API supplier for your needs.
A Bemotrizinol (USAN/INN) CoA (Certificate of Analysis) is a formal document that attests to Bemotrizinol (USAN/INN)'s compliance with Bemotrizinol (USAN/INN) specifications and serves as a tool for batch-level quality control.
Bemotrizinol (USAN/INN) CoA mostly includes findings from lab analyses of a specific batch. For each Bemotrizinol (USAN/INN) 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.
Bemotrizinol (USAN/INN) may be tested according to a variety of international standards, such as European Pharmacopoeia (Bemotrizinol (USAN/INN) EP), Bemotrizinol (USAN/INN) JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Bemotrizinol (USAN/INN) USP).