Veranova: A CDMO that manages complexity with confidence.
01 1Macfarlan Smith Limited
02 1Veranova, L.P.
03 1Noramco Coventry LLC
04 1Noramco, LLC
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 1Siegfried AG
17 1Siegfried PharmaChemikalien Minden Gmbh
18 2Siegfried USA, LLC
19 3SpecGx LLC
20 1Spectrum Chemicals and Laboratory Products
21 1TAPI Czech Industries s.r.o.
22 1Teva Czech Industries s.r.o
23 1Unichem Laboratories Limited, India
01 3BUPRENORPHINE HYDROCHLORIDE
02 1Buprenorphine
03 4Buprenorphine HCl
04 18Buprenorphine Hydrochloride
05 1Buprenorphine hydrochloride
01 1Denmark
02 1Germany
03 1India
04 3Ireland
05 1Israel
06 4Switzerland
07 13U.S.A
08 2United Kingdom
09 1Blank
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 : 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 : 49812-0182
Start Marketing Date : 1996-01-01
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 : 67509-008
Start Marketing Date : 2016-08-16
End Marketing Date : 2027-04-27
Dosage Form (Strength) : POWDER (50kg/50kg)
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 : 0792-0630
Start Marketing Date : 2011-11-16
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...
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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.
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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.
A BUNAVAIL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BUNAVAIL, including repackagers and relabelers. The FDA regulates BUNAVAIL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BUNAVAIL API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A BUNAVAIL supplier is an individual or a company that provides BUNAVAIL active pharmaceutical ingredient (API) or BUNAVAIL finished formulations upon request. The BUNAVAIL suppliers may include BUNAVAIL API manufacturers, exporters, distributors and traders.
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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 BUNAVAIL as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for BUNAVAIL 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 BUNAVAIL 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 BUNAVAIL and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a BUNAVAIL NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of BUNAVAIL suppliers with NDC on PharmaCompass.
We have 17 companies offering BUNAVAIL
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