Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Catalana SL
02 1Neuland Laboratories Limited
03 1Cambrex Profarmaco Milano Srl
01 2SOTALOL HYDROCHLORIDE
02 1Sotalol Hydrochloride
01 1India
02 1Spain
03 1U.S.A
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
NDC Package Code : 52932-0715
Start Marketing Date : 2009-10-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Neuland Laboratories- A dedicated 100% API provider.
NDC Package Code : 58032-0803
Start Marketing Date : 2017-12-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12828-0071
Start Marketing Date : 1996-12-05
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 SOTALOL HCI 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 SOTALOL HCI manufacturer or SOTALOL HCI supplier for your needs.
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PharmaCompass also assists you with knowing the SOTALOL HCI API Price utilized in the formulation of products. SOTALOL HCI API Price is not always fixed or binding as the SOTALOL HCI Price is obtained through a variety of data sources. The SOTALOL HCI Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Darob manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Darob, including repackagers and relabelers. The FDA regulates Darob manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Darob 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 Darob manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Darob supplier is an individual or a company that provides Darob active pharmaceutical ingredient (API) or Darob finished formulations upon request. The Darob suppliers may include Darob API manufacturers, exporters, distributors and traders.
click here to find a list of Darob 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 Darob as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Darob 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 Darob 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 Darob and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Darob NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Darob suppliers with NDC on PharmaCompass.
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