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Looking for 69049-06-5 / Alfentanil Hydrochloride API manufacturers, exporters & distributors?

Alfentanil Hydrochloride manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Alfentanil Hydrochloride

Synonyms

69049-06-5, Alfenta, Rapifen, Alfentanil hcl, R 39209, Alfentanil hydrochloride [usan]

Cas Number

69049-06-5

Unique Ingredient Identifier (UNII)

333JTI7A2M

About Alfentanil Hydrochloride

A short-acting opioid anesthetic and analgesic derivative of FENTANYL. It produces an early peak analgesic effect and fast recovery of consciousness. Alfentanil is effective as an anesthetic during surgery, for supplementation of analgesia during surgical procedures, and as an analgesic for critically ill patients.

Alfentanil Manufacturers

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

Alfentanil Suppliers

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

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

Alfentanil USDMF

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

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

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

Alfentanil KDMF

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

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

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

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

Alfentanil CEP

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

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

Alfentanil 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 Alfentanil as an active pharmaceutical ingredient (API).

Finished drug products

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

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

Alfentanil GMP

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

Alfentanil CoA

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

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

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