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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
  • CAPSULE;ORAL - 50,000 IU
  • 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 50-14-6 / Vitamin D API manufacturers, exporters & distributors?

Vitamin D manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Vitamin D

Synonyms

Vitamin d2, Calciferol, 50-14-6, Viosterol, Ergorone, Ercalciol

Cas Number

50-14-6

Unique Ingredient Identifier (UNII)

VS041H42XC

About Vitamin D

Derivatives of ERGOSTEROL formed by ULTRAVIOLET RAYS breaking of the C9-C10 bond. They differ from CHOLECALCIFEROL in having a double bond between C22 and C23 and a methyl group at C24.

Ergocalciferolo Manufacturers

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

Ergocalciferolo Suppliers

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

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

Ergocalciferolo USDMF

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

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

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

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

Ergocalciferolo 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 Ergocalciferolo as an active pharmaceutical ingredient (API).

Finished drug products

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

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

Ergocalciferolo GMP

Ergocalciferolo 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 Ergocalciferolo 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 Ergocalciferolo GMP manufacturer or Ergocalciferolo GMP API supplier for your needs.

Ergocalciferolo CoA

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

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

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