NDC Package Code : 71956-110
Start Marketing Date : 2024-11-22
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER, FOR SOLUTION (280mg/1)
Marketing Category : DRUG FOR FURTHER PROCESSING
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PharmaCompass offers a list of Landiolol Hydrochloride 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 Landiolol Hydrochloride manufacturer or Landiolol Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Landiolol Hydrochloride manufacturer or Landiolol Hydrochloride supplier.
PharmaCompass also assists you with knowing the Landiolol Hydrochloride API Price utilized in the formulation of products. Landiolol Hydrochloride API Price is not always fixed or binding as the Landiolol Hydrochloride Price is obtained through a variety of data sources. The Landiolol Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Landiolol Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Landiolol Hydrochloride, including repackagers and relabelers. The FDA regulates Landiolol Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Landiolol Hydrochloride 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 Landiolol Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Landiolol Hydrochloride supplier is an individual or a company that provides Landiolol Hydrochloride active pharmaceutical ingredient (API) or Landiolol Hydrochloride finished formulations upon request. The Landiolol Hydrochloride suppliers may include Landiolol Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Landiolol Hydrochloride 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 Landiolol Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Landiolol Hydrochloride 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 Landiolol Hydrochloride 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 Landiolol Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Landiolol Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Landiolol Hydrochloride suppliers with NDC on PharmaCompass.
