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  • SUPPOSITORY;RECTAL - 120MG
  • SUPPOSITORY;RECTAL - 325MG
  • SUPPOSITORY;RECTAL - 650MG
  • SUPPOSITORY;RECTAL - 80MG
  • TABLET, EXTENDED RELEASE;ORAL - 325MG;7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;ORAL - 250MG;250MG;65MG
  • TABLET;ORAL - 325MG;37.5MG
  • SOLUTION;INTRAVENOUS - 1GM/100ML (10MG/ML)
  • TABLET;ORAL - 300MG;15MG
  • TABLET;ORAL - 300MG;30MG
  • TABLET;ORAL - 300MG;60MG
  • TABLET;ORAL - 325MG;5MG
  • TABLET;ORAL - 325MG;50MG;40MG
  • TABLET;ORAL - 300MG;60MG

Looking for 103-90-2 / Paracetamol API manufacturers, exporters & distributors?

Paracetamol manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Paracetamol

Synonyms

4-acetamidophenol, 103-90-2, Tylenol, N-(4-hydroxyphenyl)acetamide, Apap, Panadol

Cas Number

103-90-2

Unique Ingredient Identifier (UNII)

362O9ITL9D

About Paracetamol

Analgesic antipyretic derivative of acetanilide. It has weak anti-inflammatory properties and is used as a common analgesic, but may cause liver, blood cell, and kidney damage.

Prestwick3_000868 Manufacturers

A Prestwick3_000868 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prestwick3_000868, including repackagers and relabelers. The FDA regulates Prestwick3_000868 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prestwick3_000868 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 Prestwick3_000868 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Prestwick3_000868 Suppliers

A Prestwick3_000868 supplier is an individual or a company that provides Prestwick3_000868 active pharmaceutical ingredient (API) or Prestwick3_000868 finished formulations upon request. The Prestwick3_000868 suppliers may include Prestwick3_000868 API manufacturers, exporters, distributors and traders.

click here to find a list of Prestwick3_000868 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Prestwick3_000868 USDMF

A Prestwick3_000868 DMF (Drug Master File) is a document detailing the whole manufacturing process of Prestwick3_000868 active pharmaceutical ingredient (API) in detail. Different forms of Prestwick3_000868 DMFs exist exist since differing nations have different regulations, such as Prestwick3_000868 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Prestwick3_000868 DMF submitted to regulatory agencies in the US is known as a USDMF. Prestwick3_000868 USDMF includes data on Prestwick3_000868's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Prestwick3_000868 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Prestwick3_000868 suppliers with USDMF on PharmaCompass.

Prestwick3_000868 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_000868 Drug Master File in Japan (Prestwick3_000868 JDMF) empowers Prestwick3_000868 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_000868 JDMF during the approval evaluation for pharmaceutical products. At the time of Prestwick3_000868 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_000868 suppliers with JDMF on PharmaCompass.

Prestwick3_000868 KDMF

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

Pharmaceutical companies submit a Prestwick3_000868 Drug Master File in Korea (Prestwick3_000868 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Prestwick3_000868. The MFDS reviews the Prestwick3_000868 KDMF as part of the drug registration process and uses the information provided in the Prestwick3_000868 KDMF to evaluate the safety and efficacy of the drug.

After submitting a Prestwick3_000868 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 Prestwick3_000868 API can apply through the Korea Drug Master File (KDMF).

click here to find a list of Prestwick3_000868 suppliers with KDMF on PharmaCompass.

Prestwick3_000868 CEP

A Prestwick3_000868 CEP of the European Pharmacopoeia monograph is often referred to as a Prestwick3_000868 Certificate of Suitability (COS). The purpose of a Prestwick3_000868 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Prestwick3_000868 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Prestwick3_000868 to their clients by showing that a Prestwick3_000868 CEP has been issued for it. The manufacturer submits a Prestwick3_000868 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Prestwick3_000868 CEP holder for the record. Additionally, the data presented in the Prestwick3_000868 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Prestwick3_000868 DMF.

A Prestwick3_000868 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Prestwick3_000868 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 Prestwick3_000868 suppliers with CEP (COS) on PharmaCompass.

Prestwick3_000868 WC

A Prestwick3_000868 written confirmation (Prestwick3_000868 WC) is an official document issued by a regulatory agency to a Prestwick3_000868 manufacturer, verifying that the manufacturing facility of a Prestwick3_000868 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Prestwick3_000868 APIs or Prestwick3_000868 finished pharmaceutical products to another nation, regulatory agencies frequently require a Prestwick3_000868 WC (written confirmation) as part of the regulatory process.

click here to find a list of Prestwick3_000868 suppliers with Written Confirmation (WC) on PharmaCompass.

Prestwick3_000868 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 Prestwick3_000868 as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Prestwick3_000868 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 Prestwick3_000868 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 Prestwick3_000868 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Prestwick3_000868 NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Prestwick3_000868 suppliers with NDC on PharmaCompass.

Prestwick3_000868 GMP

Prestwick3_000868 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_000868 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_000868 GMP manufacturer or Prestwick3_000868 GMP API supplier for your needs.

Prestwick3_000868 CoA

A Prestwick3_000868 CoA (Certificate of Analysis) is a formal document that attests to Prestwick3_000868's compliance with Prestwick3_000868 specifications and serves as a tool for batch-level quality control.

Prestwick3_000868 CoA mostly includes findings from lab analyses of a specific batch. For each Prestwick3_000868 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_000868 may be tested according to a variety of international standards, such as European Pharmacopoeia (Prestwick3_000868 EP), Prestwick3_000868 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Prestwick3_000868 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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