Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
01 1Noramco Coventry LLC
02 1Noramco, LLC
03 1Macfarlan Smith Limited
04 1Veranova, L.P.
05 1Arevipharma GmbH
06 1Cambrex Charles City, Inc
07 1Chattem Chemicals, Inc.
08 1Chr. Olesen Synthesis A/S
09 1Indivior UK Limited
10 1Janssen Pharmaceutica NV
11 1Janssen Pharmaceutical Sciences Unlimited Company
12 1LETCO MEDICAL, LLC
13 1Medisca Inc.
14 1Pharma Source Direct, Inc.
15 2Professional Compounding Centers of America
16 1SUN PHARMACEUTICAL INDUSTRIES, INC.
17 1Siegfried AG
18 1Siegfried PharmaChemikalien Minden Gmbh
19 2Siegfried USA, LLC
20 3SpecGx LLC
21 1Spectrum Chemicals and Laboratory Products
22 1TAPI Czech Industries s.r.o.
23 1Teva Czech Industries s.r.o
24 1Unichem Laboratories Limited, India
01 3BUPRENORPHINE HYDROCHLORIDE
02 1Buprenorphine
03 4Buprenorphine HCl
04 19Buprenorphine Hydrochloride
05 1Buprenorphine hydrochloride
01 1Germany
02 2India
03 3Ireland
04 1Israel
05 4Switzerland
06 13U.S.A
07 2United Kingdom
08 2Blank
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
NDC Package Code : 51634-0608
Start Marketing Date : 2017-07-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Veranova: A CDMO that manages complexity with confidence.
NDC Package Code : 12707-035
Start Marketing Date : 2017-12-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
NDC Package Code : 67509-008
Start Marketing Date : 2016-08-16
End Marketing Date : 2027-04-27
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
Veranova: A CDMO that manages complexity with confidence.
NDC Package Code : 49812-0182
Start Marketing Date : 1996-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 10920-590
Start Marketing Date : 2011-03-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0406-2910
Start Marketing Date : 2011-12-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0406-2933
Start Marketing Date : 2011-12-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0406-3210
Start Marketing Date : 2011-12-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0792-0634
Start Marketing Date : 2011-11-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 0792-0630
Start Marketing Date : 2011-11-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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.
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.
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).
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.
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.
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.
We have 17 companies offering Buprenorphine Hydrochloride
Get in contact with the supplier of your choice:
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