TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1Teva API India Private Ltd
02 1Aurobindo Pharma Limited
03 1Azico Biophore India Private Limited
04 1Maithri Drugs Private Limited
01 4Docosanol
01 3India
02 1Israel
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
NDC Package Code : 15894-0036
Start Marketing Date : 2020-10-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59651-490
Start Marketing Date : 2024-01-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69575-4024
Start Marketing Date : 2017-12-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 70600-010
Start Marketing Date : 2018-09-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Docosanol 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 Docosanol manufacturer or Docosanol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Docosanol manufacturer or Docosanol supplier.
PharmaCompass also assists you with knowing the Docosanol API Price utilized in the formulation of products. Docosanol API Price is not always fixed or binding as the Docosanol Price is obtained through a variety of data sources. The Docosanol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Stenol 1822 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Stenol 1822, including repackagers and relabelers. The FDA regulates Stenol 1822 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Stenol 1822 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 Stenol 1822 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Stenol 1822 supplier is an individual or a company that provides Stenol 1822 active pharmaceutical ingredient (API) or Stenol 1822 finished formulations upon request. The Stenol 1822 suppliers may include Stenol 1822 API manufacturers, exporters, distributors and traders.
click here to find a list of Stenol 1822 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 Stenol 1822 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Stenol 1822 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 Stenol 1822 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 Stenol 1822 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Stenol 1822 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Stenol 1822 suppliers with NDC on PharmaCompass.
We have 4 companies offering Stenol 1822
Get in contact with the supplier of your choice:
