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1. Mls002637530
2. Hydrocortisoni Acetas
3. Ncgc00183367-01
4. Chembl1715636
5. Schembl13026148
6. Hms2232p13
7. Hms3373l06
8. Bbl033683
9. Stl301800
10. Akos001582713
11. Akos021734921
12. [2-(11,17-dihydroxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1h-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl] Acetate
13. Ac-12502
14. Smr001317857
15. Vs-12217
16. Ft-0627126
17. Ft-0667894
18. Ah-034/06873032
19. Pregn-4-ene-3,20-dione,11beta,17alpha,21-trihydroxy-,21 Acetate
20. 2-(11,17-dihydroxy-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl Acetate
21. 2-{1,10-dihydroxy-9a,11a-dimethyl-7-oxo-1h,2h,3h,3ah,3bh,4h,5h,7h,8h,9h,9ah,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-1-yl}-2-oxoethyl Acetate
Molecular Weight | 404.5 g/mol |
---|---|
Molecular Formula | C23H32O6 |
XLogP3 | 2.2 |
Hydrogen Bond Donor Count | 2 |
Hydrogen Bond Acceptor Count | 6 |
Rotatable Bond Count | 4 |
Exact Mass | 404.21988874 g/mol |
Monoisotopic Mass | 404.21988874 g/mol |
Topological Polar Surface Area | 101 Ų |
Heavy Atom Count | 29 |
Formal Charge | 0 |
Complexity | 786 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 7 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
1 of 2 | |
---|---|
Drug Name | Hydrocortisone acetate |
Drug Label | Epifoam (hydrocortisone acetate 1% and pramoxine hydrochloride 1%) is a topical aerosol foam containing: hydrocortisone acetate 1% and pramoxine hydrochloride 1% in a base containing: propylene glycol, cetyl alcohol, glyceryl monostearate and PEG 1... |
Active Ingredient | Hydrocortisone acetate |
Dosage Form | Cream; Powder |
Route | For rx compounding; Topical |
Strength | 100%; 2.5% |
Market Status | Prescription |
Company | X Gen Pharms; Ferndale Labs |
2 of 2 | |
---|---|
Drug Name | Hydrocortisone acetate |
Drug Label | Epifoam (hydrocortisone acetate 1% and pramoxine hydrochloride 1%) is a topical aerosol foam containing: hydrocortisone acetate 1% and pramoxine hydrochloride 1% in a base containing: propylene glycol, cetyl alcohol, glyceryl monostearate and PEG 1... |
Active Ingredient | Hydrocortisone acetate |
Dosage Form | Cream; Powder |
Route | For rx compounding; Topical |
Strength | 100%; 2.5% |
Market Status | Prescription |
Company | X Gen Pharms; Ferndale Labs |
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Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
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PharmaCompass offers a list of Hydrocortisone Acetate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Hydrocortisone Acetate manufacturer or Hydrocortisone Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydrocortisone Acetate manufacturer or Hydrocortisone Acetate supplier.
PharmaCompass also assists you with knowing the Hydrocortisone Acetate API Price utilized in the formulation of products. Hydrocortisone Acetate API Price is not always fixed or binding as the Hydrocortisone Acetate Price is obtained through a variety of data sources. The Hydrocortisone Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A PROCTOFOAM HC manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PROCTOFOAM HC, including repackagers and relabelers. The FDA regulates PROCTOFOAM HC manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PROCTOFOAM HC 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 PROCTOFOAM HC manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A PROCTOFOAM HC supplier is an individual or a company that provides PROCTOFOAM HC active pharmaceutical ingredient (API) or PROCTOFOAM HC finished formulations upon request. The PROCTOFOAM HC suppliers may include PROCTOFOAM HC API manufacturers, exporters, distributors and traders.
click here to find a list of PROCTOFOAM HC suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A PROCTOFOAM HC DMF (Drug Master File) is a document detailing the whole manufacturing process of PROCTOFOAM HC active pharmaceutical ingredient (API) in detail. Different forms of PROCTOFOAM HC DMFs exist exist since differing nations have different regulations, such as PROCTOFOAM HC USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A PROCTOFOAM HC DMF submitted to regulatory agencies in the US is known as a USDMF. PROCTOFOAM HC USDMF includes data on PROCTOFOAM HC's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The PROCTOFOAM HC USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of PROCTOFOAM HC suppliers with USDMF 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 PROCTOFOAM HC Drug Master File in Japan (PROCTOFOAM HC JDMF) empowers PROCTOFOAM HC 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 PROCTOFOAM HC JDMF during the approval evaluation for pharmaceutical products. At the time of PROCTOFOAM HC 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 PROCTOFOAM HC suppliers with JDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a PROCTOFOAM HC Drug Master File in Korea (PROCTOFOAM HC KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of PROCTOFOAM HC. The MFDS reviews the PROCTOFOAM HC KDMF as part of the drug registration process and uses the information provided in the PROCTOFOAM HC KDMF to evaluate the safety and efficacy of the drug.
After submitting a PROCTOFOAM HC KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their PROCTOFOAM HC API can apply through the Korea Drug Master File (KDMF).
click here to find a list of PROCTOFOAM HC suppliers with KDMF on PharmaCompass.
A PROCTOFOAM HC CEP of the European Pharmacopoeia monograph is often referred to as a PROCTOFOAM HC Certificate of Suitability (COS). The purpose of a PROCTOFOAM HC CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of PROCTOFOAM HC EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of PROCTOFOAM HC to their clients by showing that a PROCTOFOAM HC CEP has been issued for it. The manufacturer submits a PROCTOFOAM HC CEP (COS) as part of the market authorization procedure, and it takes on the role of a PROCTOFOAM HC CEP holder for the record. Additionally, the data presented in the PROCTOFOAM HC CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the PROCTOFOAM HC DMF.
A PROCTOFOAM HC CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. PROCTOFOAM HC CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of PROCTOFOAM HC suppliers with CEP (COS) on PharmaCompass.
A PROCTOFOAM HC written confirmation (PROCTOFOAM HC WC) is an official document issued by a regulatory agency to a PROCTOFOAM HC manufacturer, verifying that the manufacturing facility of a PROCTOFOAM HC active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting PROCTOFOAM HC APIs or PROCTOFOAM HC finished pharmaceutical products to another nation, regulatory agencies frequently require a PROCTOFOAM HC WC (written confirmation) as part of the regulatory process.
click here to find a list of PROCTOFOAM HC suppliers with Written Confirmation (WC) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing PROCTOFOAM HC as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for PROCTOFOAM HC API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture PROCTOFOAM HC as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain PROCTOFOAM HC and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a PROCTOFOAM HC NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of PROCTOFOAM HC suppliers with NDC on PharmaCompass.
PROCTOFOAM HC 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 PROCTOFOAM HC 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 PROCTOFOAM HC GMP manufacturer or PROCTOFOAM HC GMP API supplier for your needs.
A PROCTOFOAM HC CoA (Certificate of Analysis) is a formal document that attests to PROCTOFOAM HC's compliance with PROCTOFOAM HC specifications and serves as a tool for batch-level quality control.
PROCTOFOAM HC CoA mostly includes findings from lab analyses of a specific batch. For each PROCTOFOAM HC 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.
PROCTOFOAM HC may be tested according to a variety of international standards, such as European Pharmacopoeia (PROCTOFOAM HC EP), PROCTOFOAM HC JP (Japanese Pharmacopeia) and the US Pharmacopoeia (PROCTOFOAM HC USP).