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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 anhydrous Manufacturers

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

Dexamethasone acetate anhydrous Suppliers

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

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

Dexamethasone acetate anhydrous GMP

Dexamethasone acetate anhydrous 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 anhydrous 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 anhydrous GMP manufacturer or Dexamethasone acetate anhydrous GMP API supplier for your needs.

Dexamethasone acetate anhydrous CoA

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

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