Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Catalana SL
02 1AX Pharmaceutical Corp
03 1Abhilasha Pharma Pvt. Ltd.
04 1Apex Healthcare Limited
05 1Cambrex Karlskoga AB
06 1DISHMAN CARBOGEN AMCIS LIMITED
07 1Excella GmbH & Co. KG
08 1Fagron Inc
09 1Harman Finochem Limited
10 1LETCO MEDICAL, LLC
11 1Medisca Inc.
12 1Pharma Source Direct, Inc.
13 1Professional Compounding Centers of America
14 2Professional Compounding Centers of America dba PCCA
15 1Siegfried Evionnaz SA
16 1Societa Italiana Medicinali Scandicci S.I.M.S., SrL
17 1Spectrum Laboratory Products, Inc.
18 1Willow Birch Pharma, Inc.
01 1BUPIVACAINE HCL
02 6BUPIVACAINE HYDROCHLORIDE
03 1BUPIVACAINE HYDROCHLORIDE MONOHYDRATE
04 1Bupivacaine HCL
05 4Bupivacaine HCl
06 5Bupivacaine Hydrochloride
07 1Bupivacaine Hydrochloride monohydrate
01 1Canada
02 4India
03 1Italy
04 1Luxembourg
05 1Netherlands
06 1Spain
07 1Switzerland
08 6U.S.A
09 3United Kingdom
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
NDC Package Code : 52932-0729
Start Marketing Date : 2009-09-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12651-111
Start Marketing Date : 2016-07-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-0456
Start Marketing Date : 1998-04-01
End Marketing Date : 2027-07-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 46014-1113
Start Marketing Date : 2007-12-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0524
Start Marketing Date : 2012-11-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0232
Start Marketing Date : 2022-02-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 17381-074
Start Marketing Date : 2010-05-13
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12660-0391
Start Marketing Date : 1979-02-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-1313
Start Marketing Date : 1996-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 10695-038
Start Marketing Date : 2017-04-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Bupivacaine 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 Bupivacaine Hydrochloride manufacturer or Bupivacaine Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Bupivacaine Hydrochloride API Price utilized in the formulation of products. Bupivacaine Hydrochloride API Price is not always fixed or binding as the Bupivacaine Hydrochloride Price is obtained through a variety of data sources. The Bupivacaine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Buvacaina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Buvacaina, including repackagers and relabelers. The FDA regulates Buvacaina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Buvacaina 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 Buvacaina supplier is an individual or a company that provides Buvacaina active pharmaceutical ingredient (API) or Buvacaina finished formulations upon request. The Buvacaina suppliers may include Buvacaina API manufacturers, exporters, distributors and traders.
click here to find a list of Buvacaina 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 Buvacaina as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Buvacaina 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 Buvacaina 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 Buvacaina and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Buvacaina NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Buvacaina suppliers with NDC on PharmaCompass.
We have 17 companies offering Buvacaina
Get in contact with the supplier of your choice:
