01 1Assia Chemical Industries Ltd - Teva Tech Site
02 1MSN Laboratories Private Limited
03 1YS Life Science Co., Ltd.
01 2Latanoprostene Bunod
02 1Latanoprostene bunod
01 1India
02 1Israel
03 1South Korea
NDC Package Code : 63415-0527
Start Marketing Date : 2019-07-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54893-0091
Start Marketing Date : 2019-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 40016-015
Start Marketing Date : 2024-12-17
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 Latanoprostene Bunod 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 Latanoprostene Bunod manufacturer or Latanoprostene Bunod supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Latanoprostene Bunod manufacturer or Latanoprostene Bunod supplier.
PharmaCompass also assists you with knowing the Latanoprostene Bunod API Price utilized in the formulation of products. Latanoprostene Bunod API Price is not always fixed or binding as the Latanoprostene Bunod Price is obtained through a variety of data sources. The Latanoprostene Bunod Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vyzulta manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vyzulta, including repackagers and relabelers. The FDA regulates Vyzulta manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vyzulta 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 Vyzulta manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vyzulta supplier is an individual or a company that provides Vyzulta active pharmaceutical ingredient (API) or Vyzulta finished formulations upon request. The Vyzulta suppliers may include Vyzulta API manufacturers, exporters, distributors and traders.
click here to find a list of Vyzulta 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 Vyzulta as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Vyzulta 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 Vyzulta 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 Vyzulta and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Vyzulta NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Vyzulta suppliers with NDC on PharmaCompass.
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