01 1Hainan Poly Pharm. Co., Ltd.
01 1Trimebutine Maleate
01 1China
NDC Package Code : 14335-230
Start Marketing Date : 2021-12-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
100
PharmaCompass offers a list of Trimebutine 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 Trimebutine Maleate manufacturer or Trimebutine Maleate supplier for your needs.
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PharmaCompass also assists you with knowing the Trimebutine Maleate API Price utilized in the formulation of products. Trimebutine Maleate API Price is not always fixed or binding as the Trimebutine Maleate Price is obtained through a variety of data sources. The Trimebutine Maleate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Modulon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Modulon, including repackagers and relabelers. The FDA regulates Modulon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Modulon API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Modulon supplier is an individual or a company that provides Modulon active pharmaceutical ingredient (API) or Modulon finished formulations upon request. The Modulon suppliers may include Modulon API manufacturers, exporters, distributors and traders.
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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 Modulon as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Modulon 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 Modulon 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 Modulon and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Modulon NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Modulon suppliers with NDC on PharmaCompass.
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