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Looking for 1177-87-3 / Dexamethasone Acetate API manufacturers, exporters & distributors?

Dexamethasone Acetate manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Dexamethasone 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 Dexamethasone Acetate manufacturer or Dexamethasone Acetate supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dexamethasone Acetate manufacturer or Dexamethasone Acetate supplier.

PharmaCompass also assists you with knowing the Dexamethasone Acetate API Price utilized in the formulation of products. Dexamethasone Acetate API Price is not always fixed or binding as the Dexamethasone Acetate Price is obtained through a variety of data sources. The Dexamethasone Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Dexamethasone Acetate

Synonyms

1177-87-3, Dexamethasone 21-acetate, Decadronal, Decadron-la, Panasone, Dexamethasone acetate anhydrous

Cas Number

1177-87-3

Unique Ingredient Identifier (UNII)

K7V8P532WP

About Dexamethasone Acetate

Dexamethasone Acetate is the acetate salt form of Dexamethasone, a synthetic adrenal corticosteroid with potent anti-inflammatory properties. In addition to binding to specific nuclear steroid receptors, dexamethasone also interferes with NF-kB activation and apoptotic pathways. This agent lacks the salt-retaining properties of other related adrenal hormones. (NCI04)

Dexamethasone Acetate Manufacturers

A Dexamethasone Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dexamethasone Acetate, including repackagers and relabelers. The FDA regulates Dexamethasone Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dexamethasone Acetate 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 Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Dexamethasone Acetate Suppliers

A Dexamethasone Acetate supplier is an individual or a company that provides Dexamethasone Acetate active pharmaceutical ingredient (API) or Dexamethasone Acetate finished formulations upon request. The Dexamethasone Acetate suppliers may include Dexamethasone Acetate API manufacturers, exporters, distributors and traders.

click here to find a list of Dexamethasone Acetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Dexamethasone Acetate USDMF

A Dexamethasone Acetate DMF (Drug Master File) is a document detailing the whole manufacturing process of Dexamethasone Acetate active pharmaceutical ingredient (API) in detail. Different forms of Dexamethasone Acetate DMFs exist exist since differing nations have different regulations, such as Dexamethasone Acetate USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Dexamethasone Acetate DMF submitted to regulatory agencies in the US is known as a USDMF. Dexamethasone Acetate USDMF includes data on Dexamethasone Acetate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Dexamethasone Acetate USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Dexamethasone Acetate suppliers with USDMF on PharmaCompass.

Dexamethasone Acetate CEP

A Dexamethasone Acetate CEP of the European Pharmacopoeia monograph is often referred to as a Dexamethasone Acetate Certificate of Suitability (COS). The purpose of a Dexamethasone Acetate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Dexamethasone Acetate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Dexamethasone Acetate to their clients by showing that a Dexamethasone Acetate CEP has been issued for it. The manufacturer submits a Dexamethasone Acetate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Dexamethasone Acetate CEP holder for the record. Additionally, the data presented in the Dexamethasone Acetate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Dexamethasone Acetate DMF.

A Dexamethasone Acetate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Dexamethasone Acetate 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 Acetate suppliers with CEP (COS) on PharmaCompass.

Dexamethasone Acetate NDC

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 Acetate as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Dexamethasone Acetate API and other APIs are published in this directory by the FDA.

Unfinished drugs

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 Acetate 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.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Dexamethasone Acetate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Dexamethasone Acetate NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Dexamethasone Acetate suppliers with NDC on PharmaCompass.

Dexamethasone Acetate GMP

Dexamethasone Acetate 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 Acetate 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 Acetate GMP manufacturer or Dexamethasone Acetate GMP API supplier for your needs.

Dexamethasone Acetate CoA

A Dexamethasone Acetate CoA (Certificate of Analysis) is a formal document that attests to Dexamethasone Acetate's compliance with Dexamethasone Acetate specifications and serves as a tool for batch-level quality control.

Dexamethasone Acetate CoA mostly includes findings from lab analyses of a specific batch. For each Dexamethasone Acetate 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 Acetate may be tested according to a variety of international standards, such as European Pharmacopoeia (Dexamethasone Acetate EP), Dexamethasone Acetate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Dexamethasone Acetate USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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