Close
4

Athena Athena

X

Find Frovatriptan Succinate Hydrate manufacturers, exporters & distributors on PharmaCompass

PharmaCompass
API SUPPLIERS
API Suppliers

API Suppliers

US DMFs Filed

US DMFs Filed

CEP/COS Certifications

CEP/COS Certifications

0

JDMFs Filed

JDMFs Filed

0

Other Certificates

Other Certificates

Other Suppliers

Other Suppliers

API REF. PRICE (USD / KG)

0

INTERMEDIATES

0

DOSSIERS // FDF
USA (Orange Book)

USA (Orange Book)

Europe

Europe

Canada

Canada

Australia

Australia

0

South Africa

South Africa

0

Uploaded Dossiers

Uploaded Dossiers

0

GLOBAL SALES (USD Million)

U.S. Medicaid

Annual Reports

0

EXCIPIENTS
PATENTS & EXCLUSIVITIES

USFDA Orange Book Patents

0

USFDA Exclusivities

0

DIGITAL CONTENT

Blog #PharmaFlow

0

News

REF STANDARD

EDQM

0

USP

0

JP

0

Other Listed Suppliers

0

SERVICES

0

Looking for 158930-17-7 / Frovatriptan Succinate Hydrate API manufacturers, exporters & distributors?

Frovatriptan Succinate Hydrate manufacturers, exporters & distributors 1

76

PharmaCompass offers a list of Frovatriptan Succinate Hydrate 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 Frovatriptan Succinate Hydrate manufacturer or Frovatriptan Succinate Hydrate supplier for your needs.

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

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

API | Excipient name

Frovatriptan Succinate Hydrate

Synonyms

158930-17-7, Frovatriptan succinate monohydrate, Frovatriptan succinate [usan], Frovelan, Migard, Vml 251

Cas Number

158930-17-7

Unique Ingredient Identifier (UNII)

D28J6W18HY

About Frovatriptan Succinate Hydrate

Frovatriptan Succinate is the succinate salt form of frovatriptan, a synthetic triptan with serotonin (5-HT) receptor agonist activity. Frovatriptan succinate binds selectively and with high affinity to 5-HT 1B and presynaptic 5-HT 1D receptors in the extracerebral and intracranial arteries. This leads to an inhibition of serotonin activity and results in vasoconstriction of the painfully dilated blood vessels during migraine attack. Frovatriptan succinate is indicated for the acute treatment of migraine. (NCI05)

Frovatriptan Succinate Hydrate Manufacturers

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

Frovatriptan Succinate Hydrate Suppliers

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

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

Frovatriptan Succinate Hydrate USDMF

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

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

click here to find a list of Frovatriptan Succinate Hydrate suppliers with USDMF on PharmaCompass.

Frovatriptan Succinate Hydrate KDMF

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

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

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

click here to find a list of Frovatriptan Succinate Hydrate suppliers with KDMF on PharmaCompass.

Frovatriptan Succinate Hydrate WC

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

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

Frovatriptan Succinate Hydrate 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 Frovatriptan Succinate Hydrate as an active pharmaceutical ingredient (API).

Finished drug products

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

click here to find a list of Frovatriptan Succinate Hydrate suppliers with NDC on PharmaCompass.

Frovatriptan Succinate Hydrate GMP

Frovatriptan Succinate Hydrate 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 Frovatriptan Succinate Hydrate 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 Frovatriptan Succinate Hydrate GMP manufacturer or Frovatriptan Succinate Hydrate GMP API supplier for your needs.

Frovatriptan Succinate Hydrate CoA

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

Frovatriptan Succinate Hydrate CoA mostly includes findings from lab analyses of a specific batch. For each Frovatriptan Succinate Hydrate 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.

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