01 2American Spraytech, LLC
02 3Erregierre SpA
03 1FDC Limited
04 1GUANGZHOU HANPU PHARMACEUTICAL CO LTD
05 1Janssen Pharmaceutical NV
06 1McKinley Resources Inc.
07 1Medisca Inc.
08 2Olon S.p.A.
09 1Professional Compounding Centers of America dba PCCA
10 1Quimica Sintetica S.A.
11 1Sharon Bio-Medicine Limited
12 1Spectrum Laboratory Products, Inc.
13 1Unilab Chemicals and Pharmaceuticals Private Limited
14 1Xenex Laboratories Inc
15 1YUNG ZIP CHEMICAL INDUSTRIAL CO., LTD.
16 1n.v. Ajinomoto Omnichem s.a.
01 7MICONAZOLE NITRATE
02 10Miconazole Nitrate
03 1Miconazole Nitrate Micronized
04 1Miconazole nitrate
05 1miconazole nitrate
01 1Canada
02 1China
03 3India
04 5Italy
05 1Japan
06 1Spain
07 1Taiwan
08 6U.S.A
09 1United Kingdom
NDC Package Code : 49706-5972
Start Marketing Date : 2010-01-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49706-5977
Start Marketing Date : 2010-09-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49706-5971
Start Marketing Date : 2010-01-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 43285-0288
Start Marketing Date : 2015-07-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12578-488
Start Marketing Date : 2012-04-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0038
Start Marketing Date : 2014-06-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0551
Start Marketing Date : 2024-09-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0530
Start Marketing Date : 2017-07-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-4775
Start Marketing Date : 1991-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 25119-0824
Start Marketing Date : 2018-08-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Brentan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Brentan, including repackagers and relabelers. The FDA regulates Brentan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Brentan 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 Brentan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Brentan supplier is an individual or a company that provides Brentan active pharmaceutical ingredient (API) or Brentan finished formulations upon request. The Brentan suppliers may include Brentan API manufacturers, exporters, distributors and traders.
click here to find a list of Brentan 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 Brentan as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Brentan 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 Brentan 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 Brentan and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Brentan NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Brentan suppliers with NDC on PharmaCompass.
We have 16 companies offering Brentan
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