Close
4

Athena Athena

X

Find Vitamin A Acetate manufacturers, exporters & distributors on PharmaCompass

PharmaCompass
API SUPPLIERS
API Suppliers

API Suppliers

US DMFs Filed

US DMFs Filed

CEP/COS Certifications

CEP/COS Certifications

JDMFs Filed

JDMFs Filed

Other Certificates

Other Certificates

0

Other Suppliers

Other Suppliers

API REF. PRICE (USD / KG)
84
INTERMEDIATES

0

DOSSIERS // FDF
USA (Orange Book)

USA (Orange Book)

0

Europe

Europe

0

Canada

Canada

Australia

Australia

0

South Africa

South Africa

0

Uploaded Dossiers

Uploaded Dossiers

GLOBAL SALES (USD Million)

U.S. Medicaid

0

Annual Reports

0

EXCIPIENTS
PATENTS & EXCLUSIVITIES

USFDA Orange Book Patents

0

USFDA Exclusivities

0

DIGITAL CONTENT

Blog #PharmaFlow

0

News

0

REF STANDARD

EDQM

0

USP

0

JP

Other Listed Suppliers

SERVICES

0

Looking for 127-47-9 / Vitamin A Acetate API manufacturers, exporters & distributors?

Vitamin A Acetate manufacturers, exporters & distributors 1

54

PharmaCompass offers a list of Vitamin A Acetate 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 Vitamin A Acetate manufacturer or Vitamin A Acetate supplier for your needs.

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

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

API | Excipient name

Vitamin A Acetate

Synonyms

Retinol acetate, 127-47-9, Retinol, acetate, All-trans-retinyl acetate, Crystalets, Vitamin a1 acetate

Cas Number

127-47-9

Unique Ingredient Identifier (UNII)

3LE3D9D6OY

About Vitamin A Acetate

Retinyl Acetate is a naturally-occurring fatty acid ester form of retinol (vitamin A) with potential antineoplastic and chemopreventive activities. Retinyl acetate binds to and activates retinoid receptors, inducing cell differentiation and decreasing cell proliferation. This agent also inhibits carcinogen-induced neoplastic transformation in some cancer cell types and exhibits immunomodulatory properties. (NCI04)

Vitamin A Acetate Manufacturers

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

Vitamin A Acetate Suppliers

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

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

Vitamin A Acetate USDMF

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

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

click here to find a list of Vitamin A Acetate suppliers with USDMF on PharmaCompass.

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

Vitamin A Acetate CEP

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

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

Vitamin A Acetate GMP

Vitamin A Acetate 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 Vitamin A Acetate 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 Vitamin A Acetate GMP manufacturer or Vitamin A Acetate GMP API supplier for your needs.

Vitamin A Acetate CoA

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

Vitamin A Acetate CoA mostly includes findings from lab analyses of a specific batch. For each Vitamin A Acetate 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.

Vitamin A Acetate may be tested according to a variety of international standards, such as European Pharmacopoeia (Vitamin A Acetate EP), Vitamin A Acetate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Vitamin A Acetate 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.
Ask Us for Pharmaceutical Supplier and Partner
Ask Us, Find A Supplier / Partner
No Commissions, No Strings Attached, Get Connected for FREE

What are you looking for?

How can we help you?

The request can't be empty

Please read our Privacy Policy carefully

You must agree to the privacy policy

The name can't be empty
The company can't be empty.
The email can't be empty Please enter a valid email.
The mobile can't be empty
Post Enquiry
POST ENQUIRY