Close
4

Athena Athena

X

Find Indobufen 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

0

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

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

SERVICES

0

Looking for 63610-08-2 / Indobufen API manufacturers, exporters & distributors?

Indobufen manufacturers, exporters & distributors 1

25

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

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

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

API | Excipient name

Indobufen

Synonyms

63610-08-2, Ibustrin, Indobufen [inn], K-3920, 2-[4-(3-oxo-1h-isoindol-2-yl)phenyl]butanoic acid, 6t9949g4lz

Cas Number

63610-08-2

Unique Ingredient Identifier (UNII)

6T9949G4LZ

About Indobufen

Indobufen has been used in trials studying the supportive care and prevention of Atrial Fibrillation.

Indobufen Manufacturers

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

Indobufen Suppliers

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

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

Indobufen GMP

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

Indobufen CoA

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

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

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