01 6Scientific Protein Laboratories LLC
02 1Terhormon SpA
01 1PANCRELIPASE
02 6Pancrelipase
01 1Italy
02 6U.S.A
NDC Package Code : 31387-219
Start Marketing Date : 2004-02-02
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 31387-205
Start Marketing Date : 2004-02-02
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 31387-200
Start Marketing Date : 2006-11-29
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 31387-165
Start Marketing Date : 2007-06-21
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 31387-164
Start Marketing Date : 1994-02-10
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 31387-220
Start Marketing Date : 1994-09-20
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51421-001
Start Marketing Date : 2022-07-22
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Pancrelipase API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Pancrelipase manufacturer or Pancrelipase supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pancrelipase manufacturer or Pancrelipase supplier.
A Creon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Creon, including repackagers and relabelers. The FDA regulates Creon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Creon 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 Creon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Creon supplier is an individual or a company that provides Creon active pharmaceutical ingredient (API) or Creon finished formulations upon request. The Creon suppliers may include Creon API manufacturers, exporters, distributors and traders.
click here to find a list of Creon suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Creon as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Creon 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 Creon 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 Creon and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Creon NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Creon suppliers with NDC on PharmaCompass.
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