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 : 2024-12-31
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
A Prochlorperazine Maleate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prochlorperazine Maleate, including repackagers and relabelers. The FDA regulates Prochlorperazine Maleate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prochlorperazine Maleate 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 Prochlorperazine Maleate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Prochlorperazine Maleate supplier is an individual or a company that provides Prochlorperazine Maleate active pharmaceutical ingredient (API) or Prochlorperazine Maleate finished formulations upon request. The Prochlorperazine Maleate suppliers may include Prochlorperazine Maleate API manufacturers, exporters, distributors and traders.
click here to find a list of Prochlorperazine Maleate 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 Prochlorperazine Maleate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Prochlorperazine Maleate 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 Prochlorperazine Maleate 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 Prochlorperazine Maleate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Prochlorperazine Maleate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Prochlorperazine Maleate suppliers with NDC on PharmaCompass.
We have 3 companies offering Prochlorperazine Maleate
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