Suanfarma, at the Core of a Better Life.
01 1Suanfarma Italia S.p.A
02 2Jiangsu SEL Biochem Co., LTC.
03 1Shandong Shengli Bioengineering Co.,Ltd
01 2Tiamulin Fumarate
02 1Tiamulin Hydrogen Fumarate
03 1Tiamulin fumarate
01 3China
02 1Spain
Suanfarma, at the Core of a Better Life.
NDC Package Code : 55073-0400
Start Marketing Date : 2009-12-07
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (10kg/10kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 58735-0198
Start Marketing Date : 2014-11-24
End Marketing Date : 2028-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 58735-0198
Start Marketing Date : 2014-11-24
End Marketing Date : 2028-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71783-001
Start Marketing Date : 2018-05-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Tiamulin Fumarate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tiamulin Fumarate, including repackagers and relabelers. The FDA regulates Tiamulin Fumarate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tiamulin Fumarate 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 Tiamulin Fumarate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tiamulin Fumarate supplier is an individual or a company that provides Tiamulin Fumarate active pharmaceutical ingredient (API) or Tiamulin Fumarate finished formulations upon request. The Tiamulin Fumarate suppliers may include Tiamulin Fumarate API manufacturers, exporters, distributors and traders.
click here to find a list of Tiamulin Fumarate 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 Tiamulin Fumarate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Tiamulin Fumarate 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 Tiamulin Fumarate 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 Tiamulin Fumarate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tiamulin Fumarate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Tiamulin Fumarate suppliers with NDC on PharmaCompass.
We have 3 companies offering Tiamulin Fumarate
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