01 1Anhui Haoyuan Pharmaceutical Co., Ltd. (Taodian Avenue Division)
02 1Assia Chemical Industries Ltd - Teva Tech Site
03 2CHONGQING HUAPONT SHENGCHEM PHARM. CO., INC.
04 3CHONGQING HUAPONT SHENGCHEM PHARM. CO., LTD.
05 2Cerbios-Pharma SA
06 1DARMERICA, LLC
07 2Formosa Laboratories, Inc.
08 1LETCO MEDICAL, LLC
09 1Sigma-Aldrich Corporation
01 3CALCIPOTRIENE ANHYDROUS
02 3CALCIPOTRIENE MONOHYDRATE
03 5Calcipotriene
04 1Calcipotriene Monohydrate
05 1Calcipotriol Anhydrous
06 1Calcipotriol Monohydrate
01 5China
02 1Israel
03 2Switzerland
04 2Taiwan
05 3U.S.A
06 1Blank
NDC Package Code : 63415-0052
Start Marketing Date : 2017-11-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54239-005
Start Marketing Date : 2009-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54239-015
Start Marketing Date : 2016-06-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48943-0032
Start Marketing Date : 2016-06-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48943-0026
Start Marketing Date : 2016-06-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48943-0022
Start Marketing Date : 2016-06-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48943-0030
Start Marketing Date : 2016-06-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48943-0023
Start Marketing Date : 2016-06-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-3192
Start Marketing Date : 2023-07-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 58272-197
Start Marketing Date : 2003-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Calcipotriol 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 Calcipotriol manufacturer or Calcipotriol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Calcipotriol manufacturer or Calcipotriol supplier.
PharmaCompass also assists you with knowing the Calcipotriol API Price utilized in the formulation of products. Calcipotriol API Price is not always fixed or binding as the Calcipotriol Price is obtained through a variety of data sources. The Calcipotriol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Daivonex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Daivonex, including repackagers and relabelers. The FDA regulates Daivonex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Daivonex 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 Daivonex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Daivonex supplier is an individual or a company that provides Daivonex active pharmaceutical ingredient (API) or Daivonex finished formulations upon request. The Daivonex suppliers may include Daivonex API manufacturers, exporters, distributors and traders.
click here to find a list of Daivonex suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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 Daivonex as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Daivonex API and other APIs are published in this directory by the FDA.
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 Daivonex 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.
The NDC directory also contains data on finished compounded human drug products that contain Daivonex and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Daivonex NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Daivonex suppliers with NDC on PharmaCompass.
We have 7 companies offering Daivonex
Get in contact with the supplier of your choice:
