Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
01 1Interquim, S.A. de C.V.
02 1DARMERICA, LLC
01 1Detomidine HCl
02 1Detomidine Hydrochloride
01 1Spain
02 1U.S.A
Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
NDC Package Code : 40074-0007
Start Marketing Date : 2019-12-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71052-012
Start Marketing Date : 2019-06-18
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25g/25g)
Marketing Category : BULK INGREDIENT
A Detomidine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Detomidine, including repackagers and relabelers. The FDA regulates Detomidine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Detomidine 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 Detomidine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Detomidine supplier is an individual or a company that provides Detomidine active pharmaceutical ingredient (API) or Detomidine finished formulations upon request. The Detomidine suppliers may include Detomidine API manufacturers, exporters, distributors and traders.
click here to find a list of Detomidine 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 Detomidine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Detomidine 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 Detomidine 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 Detomidine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Detomidine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Detomidine suppliers with NDC on PharmaCompass.
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