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Looking for 40828-46-4 / Suprofen API manufacturers, exporters & distributors?

Suprofen manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Suprofen

Synonyms

40828-46-4, Profenal, Sutoprofen, Suprol, P-2-thenoylhydratropic acid, Maldocil

Cas Number

40828-46-4

Unique Ingredient Identifier (UNII)

988GU2F9PE

About Suprofen

An IBUPROFEN-type anti-inflammatory analgesic and antipyretic. It inhibits prostaglandin synthesis and has been proposed as an anti-arthritic.

Prestwick3_000816 Manufacturers

A Prestwick3_000816 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prestwick3_000816, including repackagers and relabelers. The FDA regulates Prestwick3_000816 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prestwick3_000816 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

Prestwick3_000816 Suppliers

A Prestwick3_000816 supplier is an individual or a company that provides Prestwick3_000816 active pharmaceutical ingredient (API) or Prestwick3_000816 finished formulations upon request. The Prestwick3_000816 suppliers may include Prestwick3_000816 API manufacturers, exporters, distributors and traders.

click here to find a list of Prestwick3_000816 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Prestwick3_000816 USDMF

A Prestwick3_000816 DMF (Drug Master File) is a document detailing the whole manufacturing process of Prestwick3_000816 active pharmaceutical ingredient (API) in detail. Different forms of Prestwick3_000816 DMFs exist exist since differing nations have different regulations, such as Prestwick3_000816 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Prestwick3_000816 DMF submitted to regulatory agencies in the US is known as a USDMF. Prestwick3_000816 USDMF includes data on Prestwick3_000816's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Prestwick3_000816 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Prestwick3_000816 suppliers with USDMF on PharmaCompass.

Prestwick3_000816 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 Prestwick3_000816 Drug Master File in Japan (Prestwick3_000816 JDMF) empowers Prestwick3_000816 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 Prestwick3_000816 JDMF during the approval evaluation for pharmaceutical products. At the time of Prestwick3_000816 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 Prestwick3_000816 suppliers with JDMF on PharmaCompass.

Prestwick3_000816 GMP

Prestwick3_000816 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 Prestwick3_000816 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 Prestwick3_000816 GMP manufacturer or Prestwick3_000816 GMP API supplier for your needs.

Prestwick3_000816 CoA

A Prestwick3_000816 CoA (Certificate of Analysis) is a formal document that attests to Prestwick3_000816's compliance with Prestwick3_000816 specifications and serves as a tool for batch-level quality control.

Prestwick3_000816 CoA mostly includes findings from lab analyses of a specific batch. For each Prestwick3_000816 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.

Prestwick3_000816 may be tested according to a variety of international standards, such as European Pharmacopoeia (Prestwick3_000816 EP), Prestwick3_000816 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Prestwick3_000816 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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