Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
01 1Chunghwa Chemical Sysnthsis & Biotech Co.,Ltd.
02 1MSN Life Sciences Private Limited
03 1PolyPeptide Laboratories France
04 1Wisdom Pharmaceutical Co.,Ltd
01 1DIFELIKEFALIN
02 2Difelikefalin Acetate
03 1Difelikefalin acetate
01 1India
02 1Switzerland
03 1Taiwan
04 1Blank
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
NDC Package Code : 52076-6273
Start Marketing Date : 2021-12-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69766-115
Start Marketing Date : 2024-09-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59162-0002
Start Marketing Date : 2021-01-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 13612-0028
Start Marketing Date : 2025-03-27
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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A Difelikefalin Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Difelikefalin Acetate, including repackagers and relabelers. The FDA regulates Difelikefalin Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Difelikefalin Acetate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Difelikefalin Acetate supplier is an individual or a company that provides Difelikefalin Acetate active pharmaceutical ingredient (API) or Difelikefalin Acetate finished formulations upon request. The Difelikefalin Acetate suppliers may include Difelikefalin Acetate API manufacturers, exporters, distributors and traders.
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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 Difelikefalin Acetate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Difelikefalin Acetate 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 Difelikefalin Acetate 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 Difelikefalin Acetate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Difelikefalin Acetate NDC to their finished compounded human drug products, they may choose to do so.
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