Close
4

Athena Athena

X

Find Alfuzosin HCl manufacturers, exporters & distributors on PharmaCompass

PharmaCompass
API SUPPLIERS
API Suppliers

API Suppliers

US DMFs Filed

US DMFs Filed

CEP/COS Certifications

CEP/COS Certifications

JDMFs Filed

JDMFs Filed

0

Other Certificates

Other Certificates

Other Suppliers

Other Suppliers

API REF. PRICE (USD / KG)
INTERMEDIATES
DOSSIERS // FDF
USA (Orange Book)

USA (Orange Book)

Europe

Europe

Canada

Canada

Australia

Australia

South Africa

South Africa

Uploaded Dossiers

Uploaded Dossiers

GLOBAL SALES (USD Million)

U.S. Medicaid

Annual Reports

EXCIPIENTS
PATENTS & EXCLUSIVITIES

USFDA Orange Book Patents

0

USFDA Exclusivities

0

DIGITAL CONTENT

Blog #PharmaFlow

News

REF STANDARD

EDQM

USP

JP

0

Other Listed Suppliers

SERVICES

Looking for 81403-68-1 / Alfuzosin HCl API manufacturers, exporters & distributors?

Alfuzosin HCl manufacturers, exporters & distributors 1

51

PharmaCompass offers a list of Alfuzosin HCl 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 Alfuzosin HCl manufacturer or Alfuzosin HCl supplier for your needs.

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

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

API | Excipient name

Alfuzosin HCl

Synonyms

81403-68-1, Uroxatral, Urion, Xatral, Alfoten, Alfuzosin (hydrochloride)

Cas Number

81403-68-1

Unique Ingredient Identifier (UNII)

75046A1XTN

About Alfuzosin HCl

Alfuzosin Hydrochloride is the hydrochloride salt of alfuzosin, a quinazoline compound with smooth muscle-relaxing activity. Alfuzosin selectively binds to and antagonizes post-synaptic alpha-1-adrenoreceptors in smooth muscle of the prostate, bladder base, bladder neck, prostatic capsule, and prostatic urethra, initiating relaxation of smooth muscle and resulting in improvement of urine flow and the symptoms of benign prostatic hyperplasia (BPH). This agent also blocks alpha-1-adrenoreceptors in peripheral vascular smooth muscle, resulting in vasodilatation and a decrease in peripheral vascular resistance.

alphuzosine Manufacturers

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

alphuzosine Suppliers

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

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

alphuzosine USDMF

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

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

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

alphuzosine KDMF

In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.

Pharmaceutical companies submit a alphuzosine Drug Master File in Korea (alphuzosine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of alphuzosine. The MFDS reviews the alphuzosine KDMF as part of the drug registration process and uses the information provided in the alphuzosine KDMF to evaluate the safety and efficacy of the drug.

After submitting a alphuzosine 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 alphuzosine API can apply through the Korea Drug Master File (KDMF).

click here to find a list of alphuzosine suppliers with KDMF on PharmaCompass.

alphuzosine CEP

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

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

alphuzosine WC

A alphuzosine written confirmation (alphuzosine WC) is an official document issued by a regulatory agency to a alphuzosine manufacturer, verifying that the manufacturing facility of a alphuzosine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting alphuzosine APIs or alphuzosine finished pharmaceutical products to another nation, regulatory agencies frequently require a alphuzosine WC (written confirmation) as part of the regulatory process.

click here to find a list of alphuzosine suppliers with Written Confirmation (WC) on PharmaCompass.

alphuzosine 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 alphuzosine as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for alphuzosine 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 alphuzosine 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 alphuzosine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a alphuzosine NDC to their finished compounded human drug products, they may choose to do so.

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

alphuzosine GMP

alphuzosine 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 alphuzosine 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 alphuzosine GMP manufacturer or alphuzosine GMP API supplier for your needs.

alphuzosine CoA

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

alphuzosine CoA mostly includes findings from lab analyses of a specific batch. For each alphuzosine 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.

alphuzosine may be tested according to a variety of international standards, such as European Pharmacopoeia (alphuzosine EP), alphuzosine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (alphuzosine 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