Noramco Buprenorphine Hydrochloride Noramco Buprenorphine Hydrochloride

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

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Flag U.S.A
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Buprenorphine HCl
POWDER (1kg/kg)
BULK INGREDIENT
49812-0182
1996-01-01
2024-12-31
Flag U.S.A
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Buprenorphine Hydrochloride
POWDER (1g/g)
BULK INGREDIENT
12707-035
2017-12-14
2024-12-31
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Buprenorphine Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
61960-9064
2021-02-26
2025-12-31
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Buprenorphine Hydrochloride
POWDER (25kg/25kg)
BULK INGREDIENT
62756-316
2020-05-12
2024-12-31
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Buprenorphine Hydrochloride
POWDER (50kg/50kg)
BULK INGREDIENT
67509-008
2016-08-16
2027-04-27
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Buprenorphine Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
51634-0608
2017-07-26
2024-12-31
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Buprenorphine Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
73548-0608
2020-06-01
2024-03-31
Noramco

RDD 2024

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Buprenorphine hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
10920-590
2011-03-02
2025-12-31
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Buprenorphine HCl
POWDER (1kg/kg)
BULK INGREDIENT
59116-4980
2018-07-31
2024-12-31
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Buprenorphine HCl
POWDER (1mg/mg)
BULK INGREDIENT FOR ...
51552-0765
1998-04-01
2024-12-31
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Buprenorphine Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
71795-1100
2018-08-06
2025-12-31
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Buprenorphine Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
12578-608
2011-04-11
2024-12-31
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Buprenorphine Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
65267-104
2012-04-30
2024-12-31
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Buprenorphine Hydrochloride
POWDER (1g/g)
BULK INGREDIENT FOR ...
62991-1583
2011-07-20
2024-12-31
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BUPRENORPHINE HYDROCHLORIDE
POWDER (1kg/kg)
BULK INGREDIENT
0406-2910
2011-12-17
2024-12-31
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BUPRENORPHINE HYDROCHLORIDE
POWDER (1kg/kg)
BULK INGREDIENT
0406-3210
2011-12-17
2024-12-31
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BUPRENORPHINE HYDROCHLORIDE
POWDER (1kg/kg)
BULK INGREDIENT
0406-2933
2011-12-17
2024-12-31
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Buprenorphine Hydrochloride
POWDER (1g/g)
BULK INGREDIENT FOR ...
38779-0888
2014-07-28
2024-12-31
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Buprenorphine
POWDER (1kg/kg)
BULK INGREDIENT FOR ...
51927-0062
2021-04-06
2025-12-31
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BUPRENORPHINE HYDROCHLORIDE
POWDER (1kg/kg)
BULK INGREDIENT FOR ...
51927-1012
2002-07-19
2024-12-31
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Buprenorphine Hydrochloride
POWDER (1g/g)
BULK INGREDIENT FOR ...
51927-0140
2021-06-14
2025-12-31
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Buprenorphine HCl
POWDER (1kg/kg)
BULK INGREDIENT FOR ...
82393-115
2022-01-05
2024-12-31
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Buprenorphine Hydrochloride
POWDER (1kg/kg)
DRUG FOR FURTHER PRO...
65724-4521
2023-06-07
2024-12-31
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Buprenorphine Hydrochloride
POWDER (1kg/kg)
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0792-0634
2011-11-16
2024-12-31
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Buprenorphine HCl
POWDER (1kg/kg)
BULK INGREDIENT
17205-482
2007-11-12
2024-12-31
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Buprenorphine Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
0792-0630
2011-11-16
2024-12-31
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Buprenorphine Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
49452-8253
1999-07-01
2023-12-31
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Buprenorphine Hydrochloride
POWDER (100kg/100kg)
BULK INGREDIENT
47848-007
2013-03-01
2024-12-31
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Buprenorphine Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
53747-012
2009-06-30
2024-12-31
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  • INJECTABLE;INJECTION - EQ 0.3MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • IMPLANT;IMPLANTATION - EQ 80MG BASE/IMPLANT
  • FILM;BUCCAL - EQ 2.1MG BASE;EQ 0.3MG BASE
  • FILM;BUCCAL - EQ 4.2MG BASE;EQ 0.7MG BASE
  • FILM;BUCCAL - EQ 6.3MG BASE;EQ 1MG BASE
  • TABLET;SUBLINGUAL - EQ 2MG BASE;EQ 0.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET;SUBLINGUAL - EQ 8MG BASE;EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • FILM;BUCCAL - EQ 0.075MG BASE
  • FILM;BUCCAL - EQ 0.15MG BASE
  • FILM;BUCCAL - EQ 0.3MG BASE
  • FILM;BUCCAL - EQ 0.45MG BASE
  • FILM;BUCCAL - EQ 0.6MG BASE
  • FILM;BUCCAL - EQ 0.75MG BASE
  • FILM;BUCCAL - EQ 0.9MG BASE
  • FILM;BUCCAL, SUBLINGUAL - EQ 12MG BASE;EQ 3MG BASE
  • FILM;BUCCAL, SUBLINGUAL - EQ 2MG BASE;EQ 0.5MG BASE
  • FILM;BUCCAL, SUBLINGUAL - EQ 4MG BASE;EQ 1MG BASE
  • FILM;BUCCAL, SUBLINGUAL - EQ 8MG BASE;EQ 2MG BASE

Looking for 53152-21-9 / Buprenorphine Hydrochloride API manufacturers, exporters & distributors?

Buprenorphine Hydrochloride manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Buprenorphine 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 Buprenorphine Hydrochloride manufacturer or Buprenorphine Hydrochloride supplier for your needs.

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

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

API | Excipient name

Buprenorphine Hydrochloride

Synonyms

Ncgc00247733-01, Dsstox_cid_28831, Dsstox_rid_83100, Dsstox_gsid_48905, Tox21_112899, Cas-53152-21-9

Cas Number

53152-21-9

About Buprenorphine Hydrochloride

A derivative of the opioid alkaloid THEBAINE that is a more potent and longer lasting analgesic than MORPHINE. It appears to act as a partial agonist at mu and kappa opioid receptors and as an antagonist at delta receptors. The lack of delta-agonist activity has been suggested to account for the observation that buprenorphine tolerance may not develop with chronic use.

Buprenorphine Hydrochloride Manufacturers

A Buprenorphine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Buprenorphine Hydrochloride, including repackagers and relabelers. The FDA regulates Buprenorphine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Buprenorphine 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 Buprenorphine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Buprenorphine Hydrochloride Suppliers

A Buprenorphine Hydrochloride supplier is an individual or a company that provides Buprenorphine Hydrochloride active pharmaceutical ingredient (API) or Buprenorphine Hydrochloride finished formulations upon request. The Buprenorphine Hydrochloride suppliers may include Buprenorphine Hydrochloride API manufacturers, exporters, distributors and traders.

click here to find a list of Buprenorphine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Buprenorphine 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 Buprenorphine Hydrochloride as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Buprenorphine 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 Buprenorphine 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 Buprenorphine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Buprenorphine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Buprenorphine Hydrochloride suppliers with NDC on PharmaCompass.

Buprenorphine Hydrochloride Manufacturers | Traders | Suppliers

Buprenorphine 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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