Axplora- The partner of choice for complex APIs.
01 10PharmaZell GmbH
02 1Moehs Catalana SL
03 1F.I.S. Fabbrica Italiana Sintetici S.P.A.
04 1Nippon Rika Co., Ltd.
05 1Professional Compounding Centers of America dba PCCA
06 1Spectrum Laboratory Products, Inc.
01 3ACETYLCYSTEINE
02 12Acetylcysteine
01 10Germany
02 1Italy
03 1Japan
04 1Spain
05 1U.S.A
06 1United Kingdom
Axplora- The partner of choice for complex APIs.
NDC Package Code : 12598-7027
Start Marketing Date : 1995-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
NDC Package Code : 52932-0704
Start Marketing Date : 2009-09-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Axplora- The partner of choice for complex APIs.
NDC Package Code : 12598-7308
Start Marketing Date : 1995-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
Axplora- The partner of choice for complex APIs.
NDC Package Code : 12598-7308
Start Marketing Date : 1995-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Axplora- The partner of choice for complex APIs.
NDC Package Code : 12598-7311
Start Marketing Date : 1995-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Axplora- The partner of choice for complex APIs.
NDC Package Code : 12598-7311
Start Marketing Date : 1995-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Axplora- The partner of choice for complex APIs.
NDC Package Code : 12598-7323
Start Marketing Date : 1995-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Axplora- The partner of choice for complex APIs.
NDC Package Code : 12598-7027
Start Marketing Date : 1995-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Axplora- The partner of choice for complex APIs.
NDC Package Code : 12598-7294
Start Marketing Date : 1995-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
Axplora- The partner of choice for complex APIs.
NDC Package Code : 12598-7302
Start Marketing Date : 1995-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
A Mucosil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mucosil, including repackagers and relabelers. The FDA regulates Mucosil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mucosil 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 Mucosil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mucosil supplier is an individual or a company that provides Mucosil active pharmaceutical ingredient (API) or Mucosil finished formulations upon request. The Mucosil suppliers may include Mucosil API manufacturers, exporters, distributors and traders.
click here to find a list of Mucosil 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 Mucosil as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Mucosil 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 Mucosil 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 Mucosil and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Mucosil NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Mucosil suppliers with NDC on PharmaCompass.
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