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  • INJECTABLE;INTRAMUSCULAR, SUBCUTANEOUS - 0.15MG/DELIVERY
  • INJECTABLE;INTRAMUSCULAR, SUBCUTANEOUS - 0.3MG/DELIVERY
  • SOLUTION;INTRAMUSCULAR, SUBCUTANEOUS - EQ 0.15MG/DELIVERY
  • SOLUTION;INTRAMUSCULAR, SUBCUTANEOUS - EQ 0.1MG/DELIVERY
  • SOLUTION;INTRAMUSCULAR, SUBCUTANEOUS - EQ 0.3MG/DELIVERY
  • SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS - EQ 1MG BASE/ML (EQ 1MG BASE/ML)
  • SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS - 10MG/10ML (1MG/ML)
  • SOLUTION;INTRAVENOUS, INTRAOCULAR, INTRAMUSCULAR, SUBCUTANEOUS - 1MG/ML (1MG/ML)
  • SOLUTION;INTRAMUSCULAR, SUBCUTANEOUS - 0.15MG/0.3ML (0.15MG/0.3ML)
  • SOLUTION;INTRAMUSCULAR, SUBCUTANEOUS - 0.3MG/0.3ML (0.3MG/0.3ML)
  • INJECTABLE;INTRAMUSCULAR, SUBCUTANEOUS - EQ 0.15MG/DELIVERY
  • INJECTABLE;INTRAMUSCULAR, SUBCUTANEOUS - EQ 0.3MG/DELIVERY
  • INJECTABLE;INJECTION - 0.005MG/ML;0.5%
  • INJECTABLE;INJECTION - 0.005MG/ML;1%
  • INJECTABLE;INJECTION - 0.005MG/ML;1.5%
  • INJECTABLE;INJECTION - 0.005MG/ML;2%
  • INJECTABLE;INJECTION - 0.01MG/ML;1%
  • INJECTABLE;INJECTION - 0.02MG/ML;2%
  • INJECTABLE;INJECTION - 0.5%
  • INJECTABLE;INJECTION - 1%
  • INJECTABLE;INJECTION - 1.5%
  • INJECTABLE;INJECTION - 2%

Looking for 51-43-4 / Epinephrine API manufacturers, exporters & distributors?

Epinephrine manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Epinephrine

Synonyms

L-adrenaline, Adrenaline, L-epinephrine, 51-43-4, Adrenalin, Levoepinephrine

Cas Number

51-43-4

About Epinephrine

The active sympathomimetic hormone from the ADRENAL MEDULLA. It stimulates both the alpha- and beta- adrenergic systems, causes systemic VASOCONSTRICTION and gastrointestinal relaxation, stimulates the HEART, and dilates BRONCHI and cerebral vessels. It is used in ASTHMA and CARDIAC FAILURE and to delay absorption of local ANESTHETICS.

02252_FLUKA Manufacturers

A 02252_FLUKA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 02252_FLUKA, including repackagers and relabelers. The FDA regulates 02252_FLUKA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 02252_FLUKA 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 02252_FLUKA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

02252_FLUKA Suppliers

A 02252_FLUKA supplier is an individual or a company that provides 02252_FLUKA active pharmaceutical ingredient (API) or 02252_FLUKA finished formulations upon request. The 02252_FLUKA suppliers may include 02252_FLUKA API manufacturers, exporters, distributors and traders.

click here to find a list of 02252_FLUKA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

02252_FLUKA USDMF

A 02252_FLUKA DMF (Drug Master File) is a document detailing the whole manufacturing process of 02252_FLUKA active pharmaceutical ingredient (API) in detail. Different forms of 02252_FLUKA DMFs exist exist since differing nations have different regulations, such as 02252_FLUKA USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A 02252_FLUKA DMF submitted to regulatory agencies in the US is known as a USDMF. 02252_FLUKA USDMF includes data on 02252_FLUKA's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 02252_FLUKA USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of 02252_FLUKA suppliers with USDMF on PharmaCompass.

02252_FLUKA 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 02252_FLUKA Drug Master File in Japan (02252_FLUKA JDMF) empowers 02252_FLUKA 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 02252_FLUKA JDMF during the approval evaluation for pharmaceutical products. At the time of 02252_FLUKA 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 02252_FLUKA suppliers with JDMF on PharmaCompass.

02252_FLUKA CEP

A 02252_FLUKA CEP of the European Pharmacopoeia monograph is often referred to as a 02252_FLUKA Certificate of Suitability (COS). The purpose of a 02252_FLUKA CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 02252_FLUKA EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 02252_FLUKA to their clients by showing that a 02252_FLUKA CEP has been issued for it. The manufacturer submits a 02252_FLUKA CEP (COS) as part of the market authorization procedure, and it takes on the role of a 02252_FLUKA CEP holder for the record. Additionally, the data presented in the 02252_FLUKA CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 02252_FLUKA DMF.

A 02252_FLUKA CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 02252_FLUKA 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 02252_FLUKA suppliers with CEP (COS) on PharmaCompass.

02252_FLUKA WC

A 02252_FLUKA written confirmation (02252_FLUKA WC) is an official document issued by a regulatory agency to a 02252_FLUKA manufacturer, verifying that the manufacturing facility of a 02252_FLUKA active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting 02252_FLUKA APIs or 02252_FLUKA finished pharmaceutical products to another nation, regulatory agencies frequently require a 02252_FLUKA WC (written confirmation) as part of the regulatory process.

click here to find a list of 02252_FLUKA suppliers with Written Confirmation (WC) on PharmaCompass.

02252_FLUKA 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 02252_FLUKA as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for 02252_FLUKA 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 02252_FLUKA 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 02252_FLUKA and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 02252_FLUKA NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of 02252_FLUKA suppliers with NDC on PharmaCompass.

02252_FLUKA GMP

02252_FLUKA 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 02252_FLUKA 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 02252_FLUKA GMP manufacturer or 02252_FLUKA GMP API supplier for your needs.

02252_FLUKA CoA

A 02252_FLUKA CoA (Certificate of Analysis) is a formal document that attests to 02252_FLUKA's compliance with 02252_FLUKA specifications and serves as a tool for batch-level quality control.

02252_FLUKA CoA mostly includes findings from lab analyses of a specific batch. For each 02252_FLUKA 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.

02252_FLUKA may be tested according to a variety of international standards, such as European Pharmacopoeia (02252_FLUKA EP), 02252_FLUKA JP (Japanese Pharmacopeia) and the US Pharmacopoeia (02252_FLUKA 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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