Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 3FRANCOPIA
02 3Sanofi Winthrop Industrie
03 1Macfarlan Smith Limited
04 1Veranova, L.P.
05 1Siegfried AG
06 1Siegfried PharmaChemikalien Minden Gmbh
07 1Medisca Inc.
08 1Noramco, LLC
09 1Pharmaron Manufacturing Services (UK) Ltd
10 1Professional Compounding Centers of America
11 1SUN PHARMACEUTICAL INDUSTRIES, INC.
12 1Saneca Pharmaceuticals a.s.
13 2SpecGx LLC
14 1Spectrum Laboratory Products, Inc.
01 6NALOXONE HYDROCHLORIDE
02 2NALOXONE HYDROCHLORIDE DIHYDRATE
03 1Naloxone
04 1Naloxone HCl
05 1Naloxone HCl Dihydrate
06 1Naloxone HCl Ultra Fine
07 3Naloxone Hydrochloride
08 3Naloxone Hydrochloride Dihydrate
09 1Naloxone Hydrochloride dihydrate
01 6France
02 2Ireland
03 1Slovakia
04 2Switzerland
05 5U.S.A
06 1United Kingdom
07 2Blank
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
NDC Package Code : 50396-0200
Start Marketing Date : 2014-04-09
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Veranova: A CDMO that manages complexity with confidence.
NALOXONE HYDROCHLORIDE DIHYDRATE
NDC Package Code : 12707-037
Start Marketing Date : 2017-12-11
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (100g/100g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
Siegfried – A global CDMO delivering integrated pharmaceutical development and manufacturing solutions.
NDC Package Code : 17205-101
Start Marketing Date : 2010-03-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
NDC Package Code : 50396-0203
Start Marketing Date : 2020-07-20
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
NDC Package Code : 50396-0202
Start Marketing Date : 2014-04-09
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
NDC Package Code : 52465-107
Start Marketing Date : 2020-07-20
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
NDC Package Code : 52465-101
Start Marketing Date : 2014-04-09
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
NDC Package Code : 52465-102
Start Marketing Date : 2014-04-09
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Veranova: A CDMO that manages complexity with confidence.
NDC Package Code : 49812-0195
Start Marketing Date : 2012-01-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Siegfried – A global CDMO delivering integrated pharmaceutical development and manufacturing solutions.
NALOXONE HYDROCHLORIDE DIHYDRATE
NDC Package Code : 65724-0053
Start Marketing Date : 2019-05-31
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Naloxone Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Naloxone Hydrochloride manufacturer or Naloxone Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Naloxone Hydrochloride manufacturer or Naloxone Hydrochloride supplier.
A Naloxone Hydrochloride Dihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Naloxone Hydrochloride Dihydrate, including repackagers and relabelers. The FDA regulates Naloxone Hydrochloride Dihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Naloxone Hydrochloride Dihydrate 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 Naloxone Hydrochloride Dihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Naloxone Hydrochloride Dihydrate supplier is an individual or a company that provides Naloxone Hydrochloride Dihydrate active pharmaceutical ingredient (API) or Naloxone Hydrochloride Dihydrate finished formulations upon request. The Naloxone Hydrochloride Dihydrate suppliers may include Naloxone Hydrochloride Dihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Naloxone Hydrochloride Dihydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Naloxone Hydrochloride Dihydrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Naloxone Hydrochloride Dihydrate 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 Naloxone Hydrochloride Dihydrate 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 Naloxone Hydrochloride Dihydrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Naloxone Hydrochloride Dihydrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Naloxone Hydrochloride Dihydrate suppliers with NDC on PharmaCompass.
We have 9 companies offering Naloxone Hydrochloride Dihydrate
Get in contact with the supplier of your choice:
