01 2Concord Biotech Limited
02 1Fagron Inc
03 1HangZhou Zhongmei Huadong Pharmaceutical Co., Ltd
04 1Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd.
05 1LETCO MEDICAL, LLC
06 1MEDISCA Inc.
07 1Professional Compounding Centers of America
08 1Professional Compounding Centers of America dba PCCA
09 1TAPI Hungary Industries Kft.
10 1Teva Pharmaceutical Works Private Limited Company
01 1MUPIROCIN
02 10Mupirocin
01 2China
02 2India
03 1Israel
04 1Netherlands
05 2U.S.A
06 2United Kingdom
07 1Blank
NDC Package Code : 68254-0010
Start Marketing Date : 2012-07-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 68254-2504
Start Marketing Date : 2012-08-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-1194
Start Marketing Date : 2004-09-01
End Marketing Date : 2025-01-21
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 65897-1003
Start Marketing Date : 2015-03-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65897-2003
Start Marketing Date : 2021-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-2701
Start Marketing Date : 2009-06-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-2545
Start Marketing Date : 2014-08-20
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0010
Start Marketing Date : 2010-12-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0296
Start Marketing Date : 2023-04-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51846-1017
Start Marketing Date : 2019-08-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
A Mupirocin, Calcium Salt (2:1) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mupirocin, Calcium Salt (2:1), including repackagers and relabelers. The FDA regulates Mupirocin, Calcium Salt (2:1) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mupirocin, Calcium Salt (2:1) 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 Mupirocin, Calcium Salt (2:1) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mupirocin, Calcium Salt (2:1) supplier is an individual or a company that provides Mupirocin, Calcium Salt (2:1) active pharmaceutical ingredient (API) or Mupirocin, Calcium Salt (2:1) finished formulations upon request. The Mupirocin, Calcium Salt (2:1) suppliers may include Mupirocin, Calcium Salt (2:1) API manufacturers, exporters, distributors and traders.
click here to find a list of Mupirocin, Calcium Salt (2:1) 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 Mupirocin, Calcium Salt (2:1) as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Mupirocin, Calcium Salt (2:1) 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 Mupirocin, Calcium Salt (2:1) 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 Mupirocin, Calcium Salt (2:1) and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Mupirocin, Calcium Salt (2:1) NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Mupirocin, Calcium Salt (2:1) suppliers with NDC on PharmaCompass.
We have 7 companies offering Mupirocin, Calcium Salt (2:1)
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