Pluviaendo Naltrexone Hydrochloride Pluviaendo Naltrexone Hydrochloride

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List of NDC API details of Naltrexone Hydrochloride Active Pharmaceutical Ingredient listed on PharmaCompass.com

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Flag France
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NALTREXONE HYDROCHLORIDE
POWDER (1kg/kg)
BULK INGREDIENT
52465-103
2013-12-05
2025-12-31
Sanofi Company Banner

RDD 2024

Not Confirmed

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Naltrexone Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
50396-6008
2013-12-05
2024-12-31
Sanofi Company Banner

RDD 2024

Not Confirmed

envelop Contact Supplier
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Naltrexone Hydrochloride
POWDER (100g/100g)
BULK INGREDIENT FOR ...
12707-038
2017-12-11
2023-12-31
Flag Netherlands
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NA Not Available For Sales
Naltrexone Hydrochloride
POWDER (1g/g)
BULK INGREDIENT
60870-0395
1990-01-30
2024-12-31
Flag France
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Naltrexone Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
58175-0632
2019-09-01
2024-12-31
Flag India
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Naltrexone Hydrochloride
POWDER (1g/g)
BULK INGREDIENT FOR ...
70312-0887
2015-12-16
2025-12-31
Flag U.S.A
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Naltrexone Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
51634-1064
2024-01-05
2025-12-31
Flag U.S.A
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Naltrexone Hydrochloride
POWDER (1g/g)
BULK INGREDIENT FOR ...
63275-9901
2015-07-01
2025-04-01
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Naltrexone HCl Dihydrate
POWDER (1g/g)
BULK INGREDIENT FOR ...
63275-9874
2017-01-01
2025-11-01
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Naltrexone HCl
POWDER (1000g/1000g)
BULK INGREDIENT
71052-648
2020-06-25
2025-12-31
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Naltrexone HCL (Anhydrous)
POWDER (1g/g)
BULK INGREDIENT
71052-682
2021-05-17
2025-12-31
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Naltrexone Hydrochloride Dihydrate
POWDER (1g/g)
BULK INGREDIENT FOR ...
51552-1588
2021-05-25
2026-03-23
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Naltrexone Hydrochloride
POWDER (1g/g)
BULK INGREDIENT FOR ...
51552-0737
2004-09-01
2026-02-28
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NALTREXONE HYDROCHLORIDE
POWDER (1kg/kg)
BULK INGREDIENT
79572-023
2021-05-01
2024-12-31
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NALTREXONE HCL
POWDER (1g/g)
BULK INGREDIENT FOR ...
60592-552
2019-12-02
2025-12-31
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Naltrexone Hydrochloride Dihydrate
POWDER (1g/g)
BULK INGREDIENT FOR ...
62991-1243
2008-03-04
2024-12-31
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Naltrexone HCL Anhydrous
POWDER (1g/g)
BULK INGREDIENT FOR ...
62991-3125
2017-09-13
2024-12-31
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naltrexone hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
0406-1479
2013-04-15
2024-12-31
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Naltrexone Hydrochloride
POWDER (1g/g)
BULK INGREDIENT
38779-3296
2023-05-29
2024-12-31
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Naltrexone Hydrochloride
POWDER (1g/g)
BULK INGREDIENT FOR ...
38779-0887
2014-08-11
2024-12-31
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Naltrexone Hydrochloride
POWDER (1g/g)
BULK INGREDIENT
16447-0690
2023-12-01
2024-12-31
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NALTREXONE HYDROCHLORIDE
POWDER (1kg/kg)
BULK INGREDIENT FOR ...
51927-0157
2014-03-17
2025-12-31
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Naltrexone Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT FOR ...
51927-0097
2021-05-03
2025-12-31
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Naltrexone HCL
POWDER (1kg/kg)
BULK INGREDIENT
82393-111
2021-12-07
2025-12-31
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Naltrexone Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT FOR ...
69641-0001
2015-02-26
2024-12-31
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Naltrexone Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
82105-004
2023-08-03
2024-12-31
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Naltrexone Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT FOR ...
65724-0055
2020-07-15
2024-12-31
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Naltrexone Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT FOR ...
17205-108
2010-01-01
2024-12-31
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Naltrexone HCl
POWDER (1kg/kg)
BULK INGREDIENT
65724-0054
2019-02-08
2024-12-31
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Naltrexone Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
17205-103
2010-01-01
2024-12-31
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Naltrexone Hydrochloride
POWDER (1g/g)
BULK INGREDIENT
49452-4834
2001-10-01
2024-12-31
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NALTREXONE HYDROCHLORIDE
POWDER (1g/g)
BULK INGREDIENT
68981-037
2021-04-21
2024-12-31
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  • TABLET, EXTENDED RELEASE;ORAL - 90MG;8MG
  • CAPSULE, EXTENDED RELEASE;ORAL - 100MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • CAPSULE, EXTENDED RELEASE;ORAL - 20MG;0.8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • CAPSULE, EXTENDED RELEASE;ORAL - 30MG;1.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • CAPSULE, EXTENDED RELEASE;ORAL - 50MG;2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • CAPSULE, EXTENDED RELEASE;ORAL - 60MG;2.4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • CAPSULE, EXTENDED RELEASE;ORAL - 80MG;3.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Looking for 16676-29-2 / Naltrexone Hydrochloride API manufacturers, exporters & distributors?

Naltrexone Hydrochloride manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Naltrexone Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Naltrexone Hydrochloride manufacturer or Naltrexone Hydrochloride supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Naltrexone Hydrochloride manufacturer or Naltrexone Hydrochloride supplier.

PharmaCompass also assists you with knowing the Naltrexone Hydrochloride API Price utilized in the formulation of products. Naltrexone Hydrochloride API Price is not always fixed or binding as the Naltrexone Hydrochloride Price is obtained through a variety of data sources. The Naltrexone Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Naltrexone Hydrochloride

Synonyms

Naltrexone hcl, 16676-29-2, Trexan, Depade, Antaxone, Revia

Cas Number

16676-29-2

Unique Ingredient Identifier (UNII)

Z6375YW9SF

About Naltrexone Hydrochloride

Derivative of noroxymorphone that is the N-cyclopropylmethyl congener of NALOXONE. It is a narcotic antagonist that is effective orally, longer lasting and more potent than naloxone, and has been proposed for the treatment of heroin addiction. The FDA has approved naltrexone for the treatment of alcohol dependence.

Naltrexone Hydrochloride Manufacturers

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.

Naltrexone Hydrochloride Suppliers

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.

Naltrexone Hydrochloride NDC

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).

Finished drug products

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.

Unfinished drugs

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.

Compounded drug products

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.

Naltrexone Hydrochloride Manufacturers | Traders | Suppliers

Naltrexone Hydrochloride Manufacturers, Traders, Suppliers 1
Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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