Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Catalana SL
02 1Neuland Laboratories Limited
03 1Arevipharma GmbH
04 1Cambrex Profarmaco Milano Srl
01 2SOTALOL HYDROCHLORIDE
02 2Sotalol Hydrochloride
01 1Germany
02 1India
03 1Spain
04 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 : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 10920-572
Start Marketing Date : 2010-11-23
End Marketing Date : 2024-12-31
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
A Sotalol Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sotalol Hydrochloride, including repackagers and relabelers. The FDA regulates Sotalol Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sotalol 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 Sotalol Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sotalol Hydrochloride supplier is an individual or a company that provides Sotalol Hydrochloride active pharmaceutical ingredient (API) or Sotalol Hydrochloride finished formulations upon request. The Sotalol Hydrochloride suppliers may include Sotalol Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Sotalol 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 Sotalol Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sotalol 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 Sotalol 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 Sotalol Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sotalol Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sotalol Hydrochloride suppliers with NDC on PharmaCompass.
We have 4 companies offering Sotalol Hydrochloride
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