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  • FOR SOLUTION;INTRAVENOUS - 80MG/VIAL;0.02MG/VIAL;0.001MG/VIAL;5MG/VIAL;0.01MG/VIAL;0.14MG/VIAL;17MG/VIAL;0.2MG/VIAL;1MG/VIAL;1.4MG/VIAL;EQ 1.2MG BASE/VIAL;0.7MG/VIAL;7MG/VIAL
  • INJECTABLE;INTRAVENOUS - 200MG/VIAL;0.06MG/VIAL;0.005MG/VIAL;15MG/VIAL;0.005MG/VIAL;0.6MG/VIAL;40MG/VIAL;6MG/VIAL;3.6MG/VIAL;6MG/VIAL;1MG/VIAL;10MG/VIAL;0.15MG/VIAL
  • INJECTABLE;INJECTION - 20MG/ML;0.006MG/ML;0.05MCG/ML;1.5MG/ML;0.0005MG/ML;0.06MG/ML;4MG/ML;0.6MG/ML;0.36MG/ML;0.6MG/ML;0.1MG/ML;1MG/ML

Looking for 59-02-9 / Vitamin E API manufacturers, exporters & distributors?

Vitamin E manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Vitamin E

Synonyms

Alpha-tocopherol, D-alpha-tocopherol, 59-02-9, (+)-alpha-tocopherol, 5,7,8-trimethyltocol, Aquasol e

Cas Number

59-02-9

Unique Ingredient Identifier (UNII)

N9PR3490H9

About Vitamin E

A generic descriptor for all TOCOPHEROLS and TOCOTRIENOLS that exhibit ALPHA-TOCOPHEROL activity. By virtue of the phenolic hydrogen on the 2H-1-benzopyran-6-ol nucleus, these compounds exhibit varying degree of antioxidant activity, depending on the site and number of methyl groups and the type of ISOPRENOIDS.

07AA93F0-3339-4EEC-B50B-ADB70F657087 Manufacturers

A 07AA93F0-3339-4EEC-B50B-ADB70F657087 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 07AA93F0-3339-4EEC-B50B-ADB70F657087, including repackagers and relabelers. The FDA regulates 07AA93F0-3339-4EEC-B50B-ADB70F657087 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 07AA93F0-3339-4EEC-B50B-ADB70F657087 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 07AA93F0-3339-4EEC-B50B-ADB70F657087 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

07AA93F0-3339-4EEC-B50B-ADB70F657087 Suppliers

A 07AA93F0-3339-4EEC-B50B-ADB70F657087 supplier is an individual or a company that provides 07AA93F0-3339-4EEC-B50B-ADB70F657087 active pharmaceutical ingredient (API) or 07AA93F0-3339-4EEC-B50B-ADB70F657087 finished formulations upon request. The 07AA93F0-3339-4EEC-B50B-ADB70F657087 suppliers may include 07AA93F0-3339-4EEC-B50B-ADB70F657087 API manufacturers, exporters, distributors and traders.

click here to find a list of 07AA93F0-3339-4EEC-B50B-ADB70F657087 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

07AA93F0-3339-4EEC-B50B-ADB70F657087 USDMF

A 07AA93F0-3339-4EEC-B50B-ADB70F657087 DMF (Drug Master File) is a document detailing the whole manufacturing process of 07AA93F0-3339-4EEC-B50B-ADB70F657087 active pharmaceutical ingredient (API) in detail. Different forms of 07AA93F0-3339-4EEC-B50B-ADB70F657087 DMFs exist exist since differing nations have different regulations, such as 07AA93F0-3339-4EEC-B50B-ADB70F657087 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A 07AA93F0-3339-4EEC-B50B-ADB70F657087 DMF submitted to regulatory agencies in the US is known as a USDMF. 07AA93F0-3339-4EEC-B50B-ADB70F657087 USDMF includes data on 07AA93F0-3339-4EEC-B50B-ADB70F657087's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 07AA93F0-3339-4EEC-B50B-ADB70F657087 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of 07AA93F0-3339-4EEC-B50B-ADB70F657087 suppliers with USDMF on PharmaCompass.

07AA93F0-3339-4EEC-B50B-ADB70F657087 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 07AA93F0-3339-4EEC-B50B-ADB70F657087 Drug Master File in Japan (07AA93F0-3339-4EEC-B50B-ADB70F657087 JDMF) empowers 07AA93F0-3339-4EEC-B50B-ADB70F657087 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 07AA93F0-3339-4EEC-B50B-ADB70F657087 JDMF during the approval evaluation for pharmaceutical products. At the time of 07AA93F0-3339-4EEC-B50B-ADB70F657087 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 07AA93F0-3339-4EEC-B50B-ADB70F657087 suppliers with JDMF on PharmaCompass.

07AA93F0-3339-4EEC-B50B-ADB70F657087 CEP

A 07AA93F0-3339-4EEC-B50B-ADB70F657087 CEP of the European Pharmacopoeia monograph is often referred to as a 07AA93F0-3339-4EEC-B50B-ADB70F657087 Certificate of Suitability (COS). The purpose of a 07AA93F0-3339-4EEC-B50B-ADB70F657087 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 07AA93F0-3339-4EEC-B50B-ADB70F657087 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 07AA93F0-3339-4EEC-B50B-ADB70F657087 to their clients by showing that a 07AA93F0-3339-4EEC-B50B-ADB70F657087 CEP has been issued for it. The manufacturer submits a 07AA93F0-3339-4EEC-B50B-ADB70F657087 CEP (COS) as part of the market authorization procedure, and it takes on the role of a 07AA93F0-3339-4EEC-B50B-ADB70F657087 CEP holder for the record. Additionally, the data presented in the 07AA93F0-3339-4EEC-B50B-ADB70F657087 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 07AA93F0-3339-4EEC-B50B-ADB70F657087 DMF.

A 07AA93F0-3339-4EEC-B50B-ADB70F657087 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 07AA93F0-3339-4EEC-B50B-ADB70F657087 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 07AA93F0-3339-4EEC-B50B-ADB70F657087 suppliers with CEP (COS) on PharmaCompass.

07AA93F0-3339-4EEC-B50B-ADB70F657087 GMP

07AA93F0-3339-4EEC-B50B-ADB70F657087 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 07AA93F0-3339-4EEC-B50B-ADB70F657087 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 07AA93F0-3339-4EEC-B50B-ADB70F657087 GMP manufacturer or 07AA93F0-3339-4EEC-B50B-ADB70F657087 GMP API supplier for your needs.

07AA93F0-3339-4EEC-B50B-ADB70F657087 CoA

A 07AA93F0-3339-4EEC-B50B-ADB70F657087 CoA (Certificate of Analysis) is a formal document that attests to 07AA93F0-3339-4EEC-B50B-ADB70F657087's compliance with 07AA93F0-3339-4EEC-B50B-ADB70F657087 specifications and serves as a tool for batch-level quality control.

07AA93F0-3339-4EEC-B50B-ADB70F657087 CoA mostly includes findings from lab analyses of a specific batch. For each 07AA93F0-3339-4EEC-B50B-ADB70F657087 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.

07AA93F0-3339-4EEC-B50B-ADB70F657087 may be tested according to a variety of international standards, such as European Pharmacopoeia (07AA93F0-3339-4EEC-B50B-ADB70F657087 EP), 07AA93F0-3339-4EEC-B50B-ADB70F657087 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (07AA93F0-3339-4EEC-B50B-ADB70F657087 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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