01 1Lundbeck Pharmaceuticals Italy S.p.A.
01 1Imipramine Pamoate
01 1Denmark
NDC Package Code : 45562-1127
Start Marketing Date : 2008-11-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
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PharmaCompass offers a list of Imipramine 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 Imipramine manufacturer or Imipramine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Imipramine manufacturer or Imipramine supplier.
PharmaCompass also assists you with knowing the Imipramine API Price utilized in the formulation of products. Imipramine API Price is not always fixed or binding as the Imipramine Price is obtained through a variety of data sources. The Imipramine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 5,e)azepine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 5,e)azepine, including repackagers and relabelers. The FDA regulates 5,e)azepine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 5,e)azepine 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 5,e)azepine supplier is an individual or a company that provides 5,e)azepine active pharmaceutical ingredient (API) or 5,e)azepine finished formulations upon request. The 5,e)azepine suppliers may include 5,e)azepine API manufacturers, exporters, distributors and traders.
click here to find a list of 5,e)azepine 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 5,e)azepine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for 5,e)azepine 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 5,e)azepine 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 5,e)azepine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 5,e)azepine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of 5,e)azepine suppliers with NDC on PharmaCompass.
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