01 1Azico Biophore India Private Limited
02 1Medisca Inc.
03 1Trifarma S.p.A
01 2Prochlorperazine Maleate
02 1Prochlorperazine maleate
01 1India
02 1Italy
03 1U.S.A
NDC Package Code : 69575-4020
Start Marketing Date : 2017-12-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0180
Start Marketing Date : 2014-08-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46204-0106
Start Marketing Date : 2012-03-08
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 Prochlorperazine Maleate 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 Prochlorperazine Maleate manufacturer or Prochlorperazine Maleate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Prochlorperazine Maleate manufacturer or Prochlorperazine Maleate supplier.
PharmaCompass also assists you with knowing the Prochlorperazine Maleate API Price utilized in the formulation of products. Prochlorperazine Maleate API Price is not always fixed or binding as the Prochlorperazine Maleate Price is obtained through a variety of data sources. The Prochlorperazine Maleate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Emetiral manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Emetiral, including repackagers and relabelers. The FDA regulates Emetiral manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Emetiral 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 Emetiral manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Emetiral supplier is an individual or a company that provides Emetiral active pharmaceutical ingredient (API) or Emetiral finished formulations upon request. The Emetiral suppliers may include Emetiral API manufacturers, exporters, distributors and traders.
click here to find a list of Emetiral 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 Emetiral as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Emetiral 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 Emetiral 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 Emetiral and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Emetiral NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Emetiral suppliers with NDC on PharmaCompass.
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