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Looking for 52365-63-6 / Dipivefrin API manufacturers, exporters & distributors?

Dipivefrin manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Dipivefrin

Synonyms

Dipivefrine, 52365-63-6, Dipivefrinum, Dipivalyl epinephrine, Dipivefrin [usan], Dipivefrina

Cas Number

52365-63-6

Unique Ingredient Identifier (UNII)

8Q1PVL543G

About Dipivefrin

Dipivefrin is an ester prodrug of epinephrine, with sympathomimetic activity. Due to its lipophilicity, dipivefrin penetrates more easily to the anterior chamber of the eye and is hydrolyzed to epinephrine, when applied locally. Epinephrine, an adrenergic agonist, enhances the outflow of aqueous humor and decreases the production of aqueous humor by vasoconstriction. The overall result is a reduction in intraocular pressure.

Prestwick3_000632 Manufacturers

A Prestwick3_000632 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prestwick3_000632, including repackagers and relabelers. The FDA regulates Prestwick3_000632 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prestwick3_000632 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

Prestwick3_000632 Suppliers

A Prestwick3_000632 supplier is an individual or a company that provides Prestwick3_000632 active pharmaceutical ingredient (API) or Prestwick3_000632 finished formulations upon request. The Prestwick3_000632 suppliers may include Prestwick3_000632 API manufacturers, exporters, distributors and traders.

click here to find a list of Prestwick3_000632 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Prestwick3_000632 USDMF

A Prestwick3_000632 DMF (Drug Master File) is a document detailing the whole manufacturing process of Prestwick3_000632 active pharmaceutical ingredient (API) in detail. Different forms of Prestwick3_000632 DMFs exist exist since differing nations have different regulations, such as Prestwick3_000632 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Prestwick3_000632 DMF submitted to regulatory agencies in the US is known as a USDMF. Prestwick3_000632 USDMF includes data on Prestwick3_000632's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Prestwick3_000632 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Prestwick3_000632 suppliers with USDMF on PharmaCompass.

Prestwick3_000632 GMP

Prestwick3_000632 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_000632 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_000632 GMP manufacturer or Prestwick3_000632 GMP API supplier for your needs.

Prestwick3_000632 CoA

A Prestwick3_000632 CoA (Certificate of Analysis) is a formal document that attests to Prestwick3_000632's compliance with Prestwick3_000632 specifications and serves as a tool for batch-level quality control.

Prestwick3_000632 CoA mostly includes findings from lab analyses of a specific batch. For each Prestwick3_000632 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_000632 may be tested according to a variety of international standards, such as European Pharmacopoeia (Prestwick3_000632 EP), Prestwick3_000632 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Prestwick3_000632 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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