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API SUPPLIERS
Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
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Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
Human Pharmalabs manufacturer of high quality corticosteroid APIs with a state of the art facility in Kalol Gandhinagar.
Axplora is your partner of choice for complex APIs.
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Gonane has API manufacturing expertise in new-age Corticosteroids, Hormones and other pharma raw materials.
Jai Radhe Sales is your partner for all your sourcing needs.
Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
Delivering Quality APIs, Drug Intermediates, and Specialty Chemicals to Over 50 Countries Across the Globe.
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USDMF
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DOSAGE - INJECTABLE;INJECTION - EQ 4MG PHOSPH...DOSAGE - INJECTABLE;INJECTION - EQ 4MG PHOSPHATE/ML
USFDA APPLICATION NUMBER - 84916
DOSAGE - INJECTABLE;INJECTION - EQ 4MG PHOSPH...DOSAGE - INJECTABLE;INJECTION - EQ 4MG PHOSPHATE/ML
USFDA APPLICATION NUMBER - 87440
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Nanjing Well Pharmaceutical
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Nanjing Well is focused on R&D, production & sales of Pharmaceutical Excipients & Synthetic Lubricating base oils.
Dosage Form : Capsule, Cream / Lotion / Ointment, Emulsion, Gel, Injectable / Parenteral, Suspension, Tablet
Grade : Parenteral, Oral, Topical
Application : Emulsifying Agents, Film Formers & Plasticizers, Parenteral, Solubilizers, Surfactant & Foaming Agents, Thickeners and Stabilizers, Topical
Excipient Details : Polysorbate 80 is used as a plasticizer, solubilizer, emulsifier, surfactant, and suspension stabilizer. It is also used in parenteral products.
High-quality raw materials and custom blends for pharma, biopharma, nutrition, veterinary, and cosmetics worldwide.
Dosage Form : Injectable / Parenteral
Grade : Biopharma Grade
Brand Name : Citric Acid Monohydrate
Application : Parenteral, Thickeners and Stabilizers
Excipient Details : Used as a pH regulator and preservative in many Biological formulations and cell culture media. Also it can be used as a chelating agent.
Pharmacopoeia Ref : On Request
Technical Specs : Low bacteria endotoxins, low bioburden (TAMC/TYMC). Customised pa...
Ingredient(s) : Citric Acid Excipient
High-quality raw materials and custom blends for pharma, biopharma, nutrition, veterinary, and cosmetics worldwide.
Dosage Form : Injectable / Parenteral
Grade : Biopharma Grade
Application : Parenteral
Excipient Details : Used as an osmolarity agent in culture media, tonicity adjuster in ophthalmics and parenterals solutions.
Pharmacopoeia Ref : On Request
Technical Specs : Low bacteria endotoxins, low bioburden (TAMC/TYMC). Customised pa...
Ingredient(s) : Sodium Chloride Excipient
High-quality raw materials and custom blends for pharma, biopharma, nutrition, veterinary, and cosmetics worldwide.
Dosage Form : Injectable / Parenteral
Grade : Biopharma Grade
Application : Parenteral, Thickeners and Stabilizers
Excipient Details : Used as a chelating agent in cell culture media, downstream and as a chelator stabilizer in Biopharmaceutical formulations.
Pharmacopoeia Ref : On Request
Technical Specs : Low bacteria endotoxins, low bioburden (TAMC/TYMC). Customised pa...
Ingredient(s) : Disodium Edetate Excipient
Nanjing Well is focused on R&D, production & sales of Pharmaceutical Excipients & Synthetic Lubricating base oils.
Dosage Form : Cream / Lotion / Ointment, Gel, Injectable / Parenteral, Tablet
Grade : Parenteral, Oral, Topical
Application : Parenteral, Solubilizers, Topical
Excipient Details : Benzyl alcohol is used as a bacteriostatic & preservative in parenteral & ophthalmic products. It is widely used in oral & topical formulations.
High-quality raw materials and custom blends for pharma, biopharma, nutrition, veterinary, and cosmetics worldwide.
Dosage Form : Injectable / Parenteral
Grade : Biopharma Grade
Brand Name : Trisodium Citrate
Application : Parenteral
Excipient Details : Used as a buffering agent in purification process during downstream and in the final formulation.
Pharmacopoeia Ref : On Request
Technical Specs : Low bacteria endotoxins, low bioburden (TAMC/TYMC). Customised pa...
Ingredient(s) : Trisodium Citrate Excipient
High-quality raw materials and custom blends for pharma, biopharma, nutrition, veterinary, and cosmetics worldwide.
Dosage Form : Injectable / Parenteral
Grade : Biopharma Grade
Application : Parenteral, Surfactant & Foaming Agents
Excipient Details : Used as surfactant agent in cell culture media, in protein purification and in injectable formulations.
Pharmacopoeia Ref : On Request
Technical Specs : Low bacteria endotoxins, low bioburden (TAMC/TYMC). Customised pa...
Ingredient(s) : Polysorbate 80
Solubilizers
Topical
Thickeners and Stabilizers
Controlled & Modified Release
Surfactant & Foaming Agents
Nanjing Well is focused on R&D, production & sales of Pharmaceutical Excipients & Synthetic Lubricating base oils.
Dosage Form : Capsule, Cream / Lotion / Ointment, Emulsion, Gel, Injectable / Parenteral, Suspension, Tablet
Grade : Parenteral, Oral, Topical
Application : Emulsifying Agents, Film Formers & Plasticizers, Parenteral, Solubilizers, Surfactant & Foaming Agents, Thickeners and Stabilizers, Topical
Excipient Details : Polysorbate 80 is used as a plasticizer, solubilizer, emulsifier, surfactant, and suspension stabilizer. It is also used in parenteral products.
High-quality raw materials and custom blends for pharma, biopharma, nutrition, veterinary, and cosmetics worldwide.
Dosage Form : Injectable / Parenteral
Grade : Biopharma Grade
Application : Parenteral, Surfactant & Foaming Agents
Excipient Details : Used as surfactant agent in cell culture media, in protein purification and in injectable formulations.
Pharmacopoeia Ref : On Request
Technical Specs : Low bacteria endotoxins, low bioburden (TAMC/TYMC). Customised pa...
Ingredient(s) : Polysorbate 80
Emulsifying Agents
Film Formers & Plasticizers
Co-Processed Excipients
Direct Compression
Taste Masking
Rheology Modifiers
API Stability Enhancers
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PharmaCompass offers a list of Dexamethasone Sodium Phosphate 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 Dexamethasone Sodium Phosphate manufacturer or Dexamethasone Sodium Phosphate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dexamethasone Sodium Phosphate manufacturer or Dexamethasone Sodium Phosphate supplier.
PharmaCompass also assists you with knowing the Dexamethasone Sodium Phosphate API Price utilized in the formulation of products. Dexamethasone Sodium Phosphate API Price is not always fixed or binding as the Dexamethasone Sodium Phosphate Price is obtained through a variety of data sources. The Dexamethasone Sodium Phosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dexamethasone Metasulfobenzoate Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dexamethasone Metasulfobenzoate Sodium, including repackagers and relabelers. The FDA regulates Dexamethasone Metasulfobenzoate Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dexamethasone Metasulfobenzoate Sodium 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 Dexamethasone Metasulfobenzoate Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dexamethasone Metasulfobenzoate Sodium supplier is an individual or a company that provides Dexamethasone Metasulfobenzoate Sodium active pharmaceutical ingredient (API) or Dexamethasone Metasulfobenzoate Sodium finished formulations upon request. The Dexamethasone Metasulfobenzoate Sodium suppliers may include Dexamethasone Metasulfobenzoate Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Dexamethasone Metasulfobenzoate Sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dexamethasone Metasulfobenzoate Sodium DMF (Drug Master File) is a document detailing the whole manufacturing process of Dexamethasone Metasulfobenzoate Sodium active pharmaceutical ingredient (API) in detail. Different forms of Dexamethasone Metasulfobenzoate Sodium DMFs exist exist since differing nations have different regulations, such as Dexamethasone Metasulfobenzoate Sodium USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Dexamethasone Metasulfobenzoate Sodium DMF submitted to regulatory agencies in the US is known as a USDMF. Dexamethasone Metasulfobenzoate Sodium USDMF includes data on Dexamethasone Metasulfobenzoate Sodium's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Dexamethasone Metasulfobenzoate Sodium USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Dexamethasone Metasulfobenzoate Sodium 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 Dexamethasone Metasulfobenzoate Sodium Drug Master File in Japan (Dexamethasone Metasulfobenzoate Sodium JDMF) empowers Dexamethasone Metasulfobenzoate Sodium 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 Dexamethasone Metasulfobenzoate Sodium JDMF during the approval evaluation for pharmaceutical products. At the time of Dexamethasone Metasulfobenzoate Sodium 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 Dexamethasone Metasulfobenzoate Sodium 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 Dexamethasone Metasulfobenzoate Sodium Drug Master File in Korea (Dexamethasone Metasulfobenzoate Sodium KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Dexamethasone Metasulfobenzoate Sodium. The MFDS reviews the Dexamethasone Metasulfobenzoate Sodium KDMF as part of the drug registration process and uses the information provided in the Dexamethasone Metasulfobenzoate Sodium KDMF to evaluate the safety and efficacy of the drug.
After submitting a Dexamethasone Metasulfobenzoate Sodium 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 Dexamethasone Metasulfobenzoate Sodium API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Dexamethasone Metasulfobenzoate Sodium suppliers with KDMF on PharmaCompass.
A Dexamethasone Metasulfobenzoate Sodium CEP of the European Pharmacopoeia monograph is often referred to as a Dexamethasone Metasulfobenzoate Sodium Certificate of Suitability (COS). The purpose of a Dexamethasone Metasulfobenzoate Sodium CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Dexamethasone Metasulfobenzoate Sodium EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Dexamethasone Metasulfobenzoate Sodium to their clients by showing that a Dexamethasone Metasulfobenzoate Sodium CEP has been issued for it. The manufacturer submits a Dexamethasone Metasulfobenzoate Sodium CEP (COS) as part of the market authorization procedure, and it takes on the role of a Dexamethasone Metasulfobenzoate Sodium CEP holder for the record. Additionally, the data presented in the Dexamethasone Metasulfobenzoate Sodium CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Dexamethasone Metasulfobenzoate Sodium DMF.
A Dexamethasone Metasulfobenzoate Sodium CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Dexamethasone Metasulfobenzoate Sodium 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 Dexamethasone Metasulfobenzoate Sodium suppliers with CEP (COS) on PharmaCompass.
A Dexamethasone Metasulfobenzoate Sodium written confirmation (Dexamethasone Metasulfobenzoate Sodium WC) is an official document issued by a regulatory agency to a Dexamethasone Metasulfobenzoate Sodium manufacturer, verifying that the manufacturing facility of a Dexamethasone Metasulfobenzoate Sodium active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Dexamethasone Metasulfobenzoate Sodium APIs or Dexamethasone Metasulfobenzoate Sodium finished pharmaceutical products to another nation, regulatory agencies frequently require a Dexamethasone Metasulfobenzoate Sodium WC (written confirmation) as part of the regulatory process.
click here to find a list of Dexamethasone Metasulfobenzoate Sodium 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 Dexamethasone Metasulfobenzoate Sodium as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Dexamethasone Metasulfobenzoate Sodium 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 Dexamethasone Metasulfobenzoate Sodium 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 Dexamethasone Metasulfobenzoate Sodium and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Dexamethasone Metasulfobenzoate Sodium NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Dexamethasone Metasulfobenzoate Sodium suppliers with NDC on PharmaCompass.
Dexamethasone Metasulfobenzoate Sodium 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 Dexamethasone Metasulfobenzoate Sodium 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 Dexamethasone Metasulfobenzoate Sodium GMP manufacturer or Dexamethasone Metasulfobenzoate Sodium GMP API supplier for your needs.
A Dexamethasone Metasulfobenzoate Sodium CoA (Certificate of Analysis) is a formal document that attests to Dexamethasone Metasulfobenzoate Sodium's compliance with Dexamethasone Metasulfobenzoate Sodium specifications and serves as a tool for batch-level quality control.
Dexamethasone Metasulfobenzoate Sodium CoA mostly includes findings from lab analyses of a specific batch. For each Dexamethasone Metasulfobenzoate Sodium 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.
Dexamethasone Metasulfobenzoate Sodium may be tested according to a variety of international standards, such as European Pharmacopoeia (Dexamethasone Metasulfobenzoate Sodium EP), Dexamethasone Metasulfobenzoate Sodium JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Dexamethasone Metasulfobenzoate Sodium USP).
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