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