01 1CKD Bio Corporation
02 1Chongqing Daxin Pharmaceutical Co. Ltd.
03 1Concord Biotech Limited
04 1DARMERICA, LLC
05 1LETCO MEDICAL, LLC
06 2Livzon Group Fuzhou Fuxing Pharmaceutical Co., Ltd.
07 1Medisca Inc.
08 1North China Pharmaceutical Huasheng Co. Ltd.
09 1Professional Compounding Centers of America dba PCCA
10 1Spectrum Laboratory Products, Inc.
11 3Willow Birch Pharma, Inc.
12 1Xellia (Taizhou) Pharmaceuticals Co., Ltd
13 3Xellia Pharmaceuticals ApS
14 1Zhejiang Changhai Pharmaceuticals Co., Ltd.
15 1Zhejiang Medicine Co., Ltd. Xinchang Pharmaceutical Factory
01 3VANCOMYCIN HYDROCHLORIDE
02 1Vancomycin
03 3Vancomycin HCL
04 2Vancomycin HCl
05 9Vancomycin Hydrochloride
06 1Vancomycin Hydrochloride, Lyophilized
07 1Vancomycin hydrochloride
01 6China
02 4Denmark
03 1India
04 1South Korea
05 7U.S.A
06 1United Kingdom
NDC Package Code : 42513-0005
Start Marketing Date : 2013-06-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42513-0006
Start Marketing Date : 2013-06-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0274
Start Marketing Date : 2015-08-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 10695-039
Start Marketing Date : 2017-05-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 10695-039
Start Marketing Date : 2017-06-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 10695-039
Start Marketing Date : 2017-06-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 45932-0050
Start Marketing Date : 2020-06-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (7kg/7kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 44231-0001
Start Marketing Date : 1998-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 45932-0009
Start Marketing Date : 1998-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 45932-0010
Start Marketing Date : 1998-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Vancomycin Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vancomycin Hydrochloride, including repackagers and relabelers. The FDA regulates Vancomycin Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vancomycin 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 Vancomycin Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vancomycin Hydrochloride supplier is an individual or a company that provides Vancomycin Hydrochloride active pharmaceutical ingredient (API) or Vancomycin Hydrochloride finished formulations upon request. The Vancomycin Hydrochloride suppliers may include Vancomycin Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Vancomycin 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 Vancomycin Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Vancomycin 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 Vancomycin 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 Vancomycin Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Vancomycin Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Vancomycin Hydrochloride suppliers with NDC on PharmaCompass.
We have 13 companies offering Vancomycin Hydrochloride
Get in contact with the supplier of your choice:
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