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Looking for 1639-60-7 / Dextropropoxyphene HCl API manufacturers, exporters & distributors?

Dextropropoxyphene HCl manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Dextropropoxyphene HCl

Synonyms

Dextropropoxyphene hydrochloride, Algaphan, Deprancol, Darvon, Propoxyphene hcl, Dolene

Cas Number

1639-60-7

Unique Ingredient Identifier (UNII)

CB2TL9PS0T

About Dextropropoxyphene HCl

A narcotic analgesic structurally related to METHADONE. Only the dextro-isomer has an analgesic effect; the levo-isomer appears to exert an antitussive effect.

Propoxyphene Hydrochloride Manufacturers

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

Propoxyphene Hydrochloride Suppliers

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

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

Propoxyphene Hydrochloride USDMF

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

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

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

Propoxyphene Hydrochloride CEP

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

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

Propoxyphene Hydrochloride GMP

Propoxyphene Hydrochloride 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 Propoxyphene Hydrochloride 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 Propoxyphene Hydrochloride GMP manufacturer or Propoxyphene Hydrochloride GMP API supplier for your needs.

Propoxyphene Hydrochloride CoA

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

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

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