Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1FRANCOPIA
02 1Sanofi Winthrop Industrie
03 1Aspen Oss B.V.
04 1NURAY CHEMICALS PRIVATE LIMITED
05 1Wavelength Enterprises Ltd.
06 1RUSAN PHARMA LTD
07 1Deccan Nutraceuticals Pvt. Ltd.
08 1Noramco, LLC
09 1ALMON HEALTHCARE PRIVATE LIMITED
10 2B&B Pharmaceuticals, Inc.
11 2DARMERICA, LLC
12 2Fagron Inc
13 1Galenova Inc
14 1Kalchem International inc
15 2LETCO MEDICAL, LLC
16 1MEDISCA Inc.
17 1MICRO ORGO CHEM
18 2Medisca Inc.
19 3Pharma Source Direct, Inc.
20 1Professional Compounding Centers of America
21 1Professional Compounding Centers of America dba PCCA
22 1S.A.L.A.R.S. SOCIETà AZIONARIA LABORATORI ALCALOIDI RIFORNIMENTI SANITARI S.P.A.
23 1SUN PHARMACEUTICAL INDUSTRIES, INC.
24 1Saneca Pharmaceuticals a.s.
25 2Siegfried AG
26 2Siegfried PharmaChemikalien Minden Gmbh
27 1Siegfried USA, LLC
28 1SpecGx LLC
29 1Spectrum Laboratory Products, Inc.
30 1Willow Birch Pharma, INC
31 6Willow Birch Pharma, Inc
32 1Xenex Laboratories Inc
01 1NALTREXONE HCL
02 5NALTREXONE HYDROCHLORIDE
03 2Naltrexone HCL
04 1Naltrexone HCL (Anhydrous)
05 1Naltrexone HCL Anhydrous
06 2Naltrexone HCl
07 1Naltrexone HCl (Anhydrous)
08 1Naltrexone HCl (Anhydrous) (Micronized)
09 1Naltrexone HCl Dihydrate
10 24Naltrexone Hydrochloride
11 5Naltrexone Hydrochloride Dihydrate
12 1Naltrexone Hydrochloride(Nitrogen Flush)
13 1naltrexone hydrochloride
01 2Canada
02 3France
03 5India
04 1Ireland
05 1Italy
06 3Netherlands
07 1Slovakia
08 5Switzerland
09 22U.S.A
10 2United Kingdom
11 1Blank
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
NDC Package Code : 50396-6008
Start Marketing Date : 2013-12-05
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 : 60870-0395
Start Marketing Date : 1990-01-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-109
Start Marketing Date : 2024-10-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
NDC Package Code : 58175-0632
Start Marketing Date : 2019-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
NDC Package Code : 70312-0887
Start Marketing Date : 2015-12-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
Deccan Nutraceuticals: A global leader in the integrated development, manufacturing, and marketing of pharmaceutical products.
NDC Package Code : 45085-0292
Start Marketing Date : 2024-08-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
NDC Package Code : 51634-1064
Start Marketing Date : 2024-01-05
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 : 52465-103
Start Marketing Date : 2013-12-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0406-1479
Start Marketing Date : 2013-04-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0792-3941
Start Marketing Date : 2024-11-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Naltrexone Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Naltrexone Hydrochloride, including repackagers and relabelers. The FDA regulates Naltrexone Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Naltrexone 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 Naltrexone Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Naltrexone Hydrochloride supplier is an individual or a company that provides Naltrexone Hydrochloride active pharmaceutical ingredient (API) or Naltrexone Hydrochloride finished formulations upon request. The Naltrexone Hydrochloride suppliers may include Naltrexone Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Naltrexone 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 Naltrexone Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Naltrexone 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 Naltrexone 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 Naltrexone Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Naltrexone Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Naltrexone Hydrochloride suppliers with NDC on PharmaCompass.
We have 25 companies offering Naltrexone Hydrochloride
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