With Fermion, start the journey of your innovative API.
01 1Fermion Oy
02 1Interquim S.A. de C.V.
03 1Interquim, S.A. de C.V.
04 1Moehs Iberica SL
05 2NORCHIM
06 1Supriya Lifescience Limited
07 1Asymchem Laboratories (Tianjin) Co., Ltd.
08 1Edmond Pharma Srl
09 1Emcure Pharmaceuticals Limited
10 1Guang’an Kingday Pharma & Chem Co., Ltd.
11 1Hubei Biocause Heilen Pharmaceutical Co., Ltd
12 1Jiangsu Hengrui Pharmaceuticals Co., Ltd.
13 1Maithri Drugs Private Limited
14 1Sterling Pharma Solutions Limited
15 1Strem Chemicals, Inc.
01 1DEXMEDETOMIDINE
02 3DEXMEDETOMIDINE HYDROCHLORIDE
03 1Dexmedetomidine HCI
04 2Dexmedetomidine HCl
05 7Dexmedetomidine Hydrochloride
06 1Medetomidine Hydrochloride
07 1dexmedetomidine hydrochloride
01 4China
02 1Finland
03 2France
04 3India
05 3Spain
06 1Sweden
07 1U.S.A
08 1United Kingdom
With Fermion, start the journey of your innovative API.
NDC Package Code : 12780-4640
Start Marketing Date : 1998-10-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
NDC Package Code : 40074-0004
Start Marketing Date : 2018-11-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
NDC Package Code : 81912-0001
Start Marketing Date : 2021-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 56087-0001
Start Marketing Date : 2019-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
NDC Package Code : 61281-9800
Start Marketing Date : 2023-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
NDC Package Code : 40074-0006
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 : 56087-0002
Start Marketing Date : 2019-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14593-887
Start Marketing Date : 2022-06-02
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50384-0100
Start Marketing Date : 2009-03-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (350g/350g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50711-0008
Start Marketing Date : 2012-03-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Dexmedetomidine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dexmedetomidine Hydrochloride, including repackagers and relabelers. The FDA regulates Dexmedetomidine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dexmedetomidine 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 Dexmedetomidine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dexmedetomidine Hydrochloride supplier is an individual or a company that provides Dexmedetomidine Hydrochloride active pharmaceutical ingredient (API) or Dexmedetomidine Hydrochloride finished formulations upon request. The Dexmedetomidine Hydrochloride suppliers may include Dexmedetomidine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Dexmedetomidine 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 Dexmedetomidine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Dexmedetomidine 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 Dexmedetomidine 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 Dexmedetomidine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Dexmedetomidine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Dexmedetomidine Hydrochloride suppliers with NDC on PharmaCompass.
We have 14 companies offering Dexmedetomidine Hydrochloride
Get in contact with the supplier of your choice:
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