01 1N R Oils
02 1NR OILS
01 2Antifungal Drug Substance
01 2India
NDC Package Code : 81466-504
Start Marketing Date : 2021-04-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (60kg/60kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 81466-504
Start Marketing Date : 2022-02-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
A Zinc Undecylenate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zinc Undecylenate, including repackagers and relabelers. The FDA regulates Zinc Undecylenate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zinc Undecylenate 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 Zinc Undecylenate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zinc Undecylenate supplier is an individual or a company that provides Zinc Undecylenate active pharmaceutical ingredient (API) or Zinc Undecylenate finished formulations upon request. The Zinc Undecylenate suppliers may include Zinc Undecylenate API manufacturers, exporters, distributors and traders.
click here to find a list of Zinc Undecylenate 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 Zinc Undecylenate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Zinc Undecylenate 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 Zinc Undecylenate 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 Zinc Undecylenate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Zinc Undecylenate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Zinc Undecylenate suppliers with NDC on PharmaCompass.
We have 1 companies offering Zinc Undecylenate
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