Close
4

Athena Athena

X

Find Dexamethasone Valerate manufacturers, exporters & distributors on PharmaCompass

PharmaCompass
API SUPPLIERS
API Suppliers

API Suppliers

US DMFs Filed

US DMFs Filed

0

CEP/COS Certifications

CEP/COS Certifications

0

JDMFs Filed

JDMFs Filed

Other Certificates

Other Certificates

0

Other Suppliers

Other Suppliers

API REF. PRICE (USD / KG)

0

INTERMEDIATES

0

DOSSIERS // FDF
USA (Orange Book)

USA (Orange Book)

0

Europe

Europe

0

Canada

Canada

0

Australia

Australia

0

South Africa

South Africa

0

Uploaded Dossiers

Uploaded Dossiers

0

GLOBAL SALES (USD Million)

U.S. Medicaid

0

Annual Reports

0

EXCIPIENTS

0

PATENTS & EXCLUSIVITIES

USFDA Orange Book Patents

0

USFDA Exclusivities

0

DIGITAL CONTENT

Blog #PharmaFlow

0

News

0

REF STANDARD

EDQM

0

USP

0

JP

0

Other Listed Suppliers

0

SERVICES

0

Looking for 33755-46-3 / Dexamethasone Valerate API manufacturers, exporters & distributors?

Dexamethasone Valerate manufacturers, exporters & distributors 1

57

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

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

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

API | Excipient name

Dexamethasone Valerate

Synonyms

33755-46-3, Dexamethasone 17-valerate, Dv-17, Dexamethasone valerate [jan], Oi7cp949nn, [(8s,9r,10s,11s,13s,14s,16r,17r)-9-fluoro-11-hydroxy-17-(2-hydroxyacetyl)-10,13,16-trimethyl-3-oxo-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-17-yl] pentanoate

Cas Number

33755-46-3

Unique Ingredient Identifier (UNII)

OI7CP949NN

Dexamethasone 17-valerate Manufacturers

A Dexamethasone 17-valerate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dexamethasone 17-valerate, including repackagers and relabelers. The FDA regulates Dexamethasone 17-valerate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dexamethasone 17-valerate 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 17-valerate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Dexamethasone 17-valerate Suppliers

A Dexamethasone 17-valerate supplier is an individual or a company that provides Dexamethasone 17-valerate active pharmaceutical ingredient (API) or Dexamethasone 17-valerate finished formulations upon request. The Dexamethasone 17-valerate suppliers may include Dexamethasone 17-valerate API manufacturers, exporters, distributors and traders.

click here to find a list of Dexamethasone 17-valerate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Dexamethasone 17-valerate JDMF

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 17-valerate Drug Master File in Japan (Dexamethasone 17-valerate JDMF) empowers Dexamethasone 17-valerate 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 17-valerate JDMF during the approval evaluation for pharmaceutical products. At the time of Dexamethasone 17-valerate 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 17-valerate suppliers with JDMF on PharmaCompass.

Dexamethasone 17-valerate GMP

Dexamethasone 17-valerate 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 17-valerate 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 17-valerate GMP manufacturer or Dexamethasone 17-valerate GMP API supplier for your needs.

Dexamethasone 17-valerate CoA

A Dexamethasone 17-valerate CoA (Certificate of Analysis) is a formal document that attests to Dexamethasone 17-valerate's compliance with Dexamethasone 17-valerate specifications and serves as a tool for batch-level quality control.

Dexamethasone 17-valerate CoA mostly includes findings from lab analyses of a specific batch. For each Dexamethasone 17-valerate 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 17-valerate may be tested according to a variety of international standards, such as European Pharmacopoeia (Dexamethasone 17-valerate EP), Dexamethasone 17-valerate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Dexamethasone 17-valerate 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.
Ask Us for Pharmaceutical Supplier and Partner
Ask Us, Find A Supplier / Partner
No Commissions, No Strings Attached, Get Connected for FREE

What are you looking for?

How can we help you?

The request can't be empty

Please read our Privacy Policy carefully

You must agree to the privacy policy

The name can't be empty
The company can't be empty.
The email can't be empty Please enter a valid email.
The mobile can't be empty
Post Enquiry
POST ENQUIRY