01 1CAMBREX PROFARMACO MILANO SRL
01 1AMBROXOL HCL
01 1U.S.A
NDC Package Code : 12828-0093
Start Marketing Date : 2022-08-04
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 Ambroxol 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 Ambroxol Hydrochloride manufacturer or Ambroxol Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ambroxol Hydrochloride manufacturer or Ambroxol Hydrochloride supplier.
PharmaCompass also assists you with knowing the Ambroxol Hydrochloride API Price utilized in the formulation of products. Ambroxol Hydrochloride API Price is not always fixed or binding as the Ambroxol Hydrochloride Price is obtained through a variety of data sources. The Ambroxol Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lazolvan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lazolvan, including repackagers and relabelers. The FDA regulates Lazolvan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lazolvan 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 Lazolvan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lazolvan supplier is an individual or a company that provides Lazolvan active pharmaceutical ingredient (API) or Lazolvan finished formulations upon request. The Lazolvan suppliers may include Lazolvan API manufacturers, exporters, distributors and traders.
click here to find a list of Lazolvan 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 Lazolvan as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Lazolvan 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 Lazolvan 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 Lazolvan and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Lazolvan NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Lazolvan suppliers with NDC on PharmaCompass.
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