01 1Inner Mongolia ZM Bio-pharmaceutical Co.,Ltd
01 1tylvalosin tartrate
01 1China
NDC Package Code : 81474-001
Start Marketing Date : 2023-01-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Tylvalosin Tartrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tylvalosin Tartrate, including repackagers and relabelers. The FDA regulates Tylvalosin Tartrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tylvalosin Tartrate 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 Tylvalosin Tartrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tylvalosin Tartrate supplier is an individual or a company that provides Tylvalosin Tartrate active pharmaceutical ingredient (API) or Tylvalosin Tartrate finished formulations upon request. The Tylvalosin Tartrate suppliers may include Tylvalosin Tartrate API manufacturers, exporters, distributors and traders.
click here to find a list of Tylvalosin Tartrate 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 Tylvalosin Tartrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Tylvalosin Tartrate 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 Tylvalosin Tartrate 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 Tylvalosin Tartrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tylvalosin Tartrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Tylvalosin Tartrate suppliers with NDC on PharmaCompass.
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