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API SUPPLIERS
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EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Regulatory Info :
Registration Country : Sweden
Brand Name : Lomudal
Dosage Form : INHALATION, SUSPENSION
Dosage Strength : 5 MG / DOSE
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Registration Country : Sweden
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Regulatory Info :
Registration Country : Sweden
Brand Name : Lomudal nasal
Dosage Form : NASAL SPRAY, SOLUTION
Dosage Strength : 2.6 MG / DOSE
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Registration Country : Sweden
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Sweden
Brand Name : Lomudal
Dosage Form : EYE DROPS, SOLUTION IN SINGLE-DOSE CONTAINERS
Dosage Strength : 40 MG / ML
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Regulatory Info :
Registration Country : Sweden
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Sweden
Brand Name : Lomudal
Dosage Form : EYE DROPS, SOLUTION
Dosage Strength : 20 MG / ML
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Approval Date :
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Regulatory Info :
Registration Country : Sweden
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Sweden
Brand Name : Lomudal
Dosage Form : INHALATION POWDER, HARD CAPSULE
Dosage Strength : 20 MG
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Registration Country : Sweden
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Sweden
Brand Name : Lomudal GI
Dosage Form : ORAL SOLUTION
Dosage Strength : 20 MG / ML
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Regulatory Info :
Registration Country : Sweden
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
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Registration Country : Italy
Brand Name : Lomudal
Dosage Form :
Dosage Strength : Coll 10 Ml 4%
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Registration Country : Italy
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
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Registration Country : Italy
Brand Name : Lomudal
Dosage Form :
Dosage Strength : 24 Vials 20 Mg 2 Ml Aerosol
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Registration Country : Italy
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Norway
Brand Name : Lomudal
Dosage Form : Eye drops, resolution
Dosage Strength : 20 mg/ml
Packaging : Bottle
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Norway
Brand Name : Lomudal
Dosage Form : Eye drops, resolution
Dosage Strength : 40 mg/ml
Packaging : Pipette, endose
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
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REF. STANDARDS & IMPURITIES
EDQM
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USP reference standards; highly characterized specimens of drug substances, impurities, excipients, degradation products & more.
CAS Number : 699-83-2
Quantity Per Vial :
Price ($) : 850
Catalog Number : 1A06030
Current Lot : 25 mg
Previous Lot :
NDC Code :
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PharmaCompass offers a list of Sodium Cromoglicate 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 Sodium Cromoglicate manufacturer or Sodium Cromoglicate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Cromoglicate manufacturer or Sodium Cromoglicate supplier.
PharmaCompass also assists you with knowing the Sodium Cromoglicate API Price utilized in the formulation of products. Sodium Cromoglicate API Price is not always fixed or binding as the Sodium Cromoglicate Price is obtained through a variety of data sources. The Sodium Cromoglicate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cromolyn sodium (USP) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cromolyn sodium (USP), including repackagers and relabelers. The FDA regulates Cromolyn sodium (USP) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cromolyn sodium (USP) 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 Cromolyn sodium (USP) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cromolyn sodium (USP) supplier is an individual or a company that provides Cromolyn sodium (USP) active pharmaceutical ingredient (API) or Cromolyn sodium (USP) finished formulations upon request. The Cromolyn sodium (USP) suppliers may include Cromolyn sodium (USP) API manufacturers, exporters, distributors and traders.
click here to find a list of Cromolyn sodium (USP) suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cromolyn sodium (USP) DMF (Drug Master File) is a document detailing the whole manufacturing process of Cromolyn sodium (USP) active pharmaceutical ingredient (API) in detail. Different forms of Cromolyn sodium (USP) DMFs exist exist since differing nations have different regulations, such as Cromolyn sodium (USP) USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cromolyn sodium (USP) DMF submitted to regulatory agencies in the US is known as a USDMF. Cromolyn sodium (USP) USDMF includes data on Cromolyn sodium (USP)'s chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cromolyn sodium (USP) USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cromolyn sodium (USP) 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 Cromolyn sodium (USP) Drug Master File in Japan (Cromolyn sodium (USP) JDMF) empowers Cromolyn sodium (USP) 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 Cromolyn sodium (USP) JDMF during the approval evaluation for pharmaceutical products. At the time of Cromolyn sodium (USP) 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 Cromolyn sodium (USP) suppliers with JDMF on PharmaCompass.
A Cromolyn sodium (USP) CEP of the European Pharmacopoeia monograph is often referred to as a Cromolyn sodium (USP) Certificate of Suitability (COS). The purpose of a Cromolyn sodium (USP) CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cromolyn sodium (USP) EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cromolyn sodium (USP) to their clients by showing that a Cromolyn sodium (USP) CEP has been issued for it. The manufacturer submits a Cromolyn sodium (USP) CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cromolyn sodium (USP) CEP holder for the record. Additionally, the data presented in the Cromolyn sodium (USP) CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cromolyn sodium (USP) DMF.
A Cromolyn sodium (USP) CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cromolyn sodium (USP) 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 Cromolyn sodium (USP) suppliers with CEP (COS) 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 Cromolyn sodium (USP) as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cromolyn sodium (USP) 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 Cromolyn sodium (USP) 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 Cromolyn sodium (USP) and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cromolyn sodium (USP) NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cromolyn sodium (USP) suppliers with NDC on PharmaCompass.
Cromolyn sodium (USP) 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 Cromolyn sodium (USP) 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 Cromolyn sodium (USP) GMP manufacturer or Cromolyn sodium (USP) GMP API supplier for your needs.
A Cromolyn sodium (USP) CoA (Certificate of Analysis) is a formal document that attests to Cromolyn sodium (USP)'s compliance with Cromolyn sodium (USP) specifications and serves as a tool for batch-level quality control.
Cromolyn sodium (USP) CoA mostly includes findings from lab analyses of a specific batch. For each Cromolyn sodium (USP) 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.
Cromolyn sodium (USP) may be tested according to a variety of international standards, such as European Pharmacopoeia (Cromolyn sodium (USP) EP), Cromolyn sodium (USP) JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Cromolyn sodium (USP) USP).
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