Veranova: A CDMO that manages complexity with confidence.
01 1Macfarlan Smith Limited
02 1Veranova, L.P.
03 3FRANCOPIA
04 3Sanofi Winthrop Industrie
05 1Aspen Oss B.V.
06 1Medisca Inc.
07 1Pharmaron Manufacturing Services (UK) Ltd
08 1Professional Compounding Centers of America
09 1Saneca Pharmaceuticals a.s.
10 1Siegfried AG
11 1Siegfried PharmaChemikalien Minden Gmbh
12 2SpecGx LLC
13 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 4Naloxone Hydrochloride
08 2Naloxone Hydrochloride Dihydrate
01 6France
02 2Ireland
03 1Netherlands
04 1Slovakia
05 2Switzerland
06 5U.S.A
07 1United Kingdom
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 : 2025-12-31
Dosage Form (Strength) : POWDER (100g/100g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
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 : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Aspen API. More than just an API.
NDC Package Code : 60870-0288
Start Marketing Date : 1986-10-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
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 : 2024-12-31
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 : 2025-12-31
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 : 2025-12-31
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 : 2025-12-31
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 : 2025-12-31
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 : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0406-1492
Start Marketing Date : 2013-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Naloxone Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Naloxone Hydrochloride, including repackagers and relabelers. The FDA regulates Naloxone Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Naloxone 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 Naloxone Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Naloxone Hydrochloride supplier is an individual or a company that provides Naloxone Hydrochloride active pharmaceutical ingredient (API) or Naloxone Hydrochloride finished formulations upon request. The Naloxone Hydrochloride suppliers may include Naloxone Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Naloxone 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 Naloxone Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Naloxone 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 Naloxone 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 Naloxone Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Naloxone Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Naloxone Hydrochloride suppliers with NDC on PharmaCompass.
We have 10 companies offering Naloxone Hydrochloride
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