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Looking for 1225-55-4 / Protriptyline API manufacturers, exporters & distributors?

Protriptyline manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Protriptyline

Synonyms

1225-55-4, Protriptyline hcl, Concordin, Maximed, Protriptyline (hydrochloride), Triptyl

Cas Number

1225-55-4

Unique Ingredient Identifier (UNII)

44665V00O8

About Protriptyline

Tricyclic antidepressant similar in action and side effects to IMIPRAMINE. It may produce excitation.

Protriptyline Hydrochloride Manufacturers

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

Protriptyline Hydrochloride Suppliers

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

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

Protriptyline Hydrochloride USDMF

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

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

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

Protriptyline Hydrochloride 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 Protriptyline Hydrochloride as an active pharmaceutical ingredient (API).

Finished drug products

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

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

Protriptyline Hydrochloride GMP

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

Protriptyline Hydrochloride CoA

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

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

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