01 2Hebei Jiheng Pharmaceutical Co., Ltd.
02 1Sinopep-Allsino Biopharmaceutical Co., Ltd.
01 1dinitolmide
02 1dinitomide
03 1zoalene
01 3China
NDC Package Code : 81919-009
Start Marketing Date : 2022-01-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 81919-008
Start Marketing Date : 2021-09-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 76177-180
Start Marketing Date : 2019-01-31
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Zoalene manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zoalene, including repackagers and relabelers. The FDA regulates Zoalene manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zoalene API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Zoalene supplier is an individual or a company that provides Zoalene active pharmaceutical ingredient (API) or Zoalene finished formulations upon request. The Zoalene suppliers may include Zoalene API manufacturers, exporters, distributors and traders.
click here to find a list of Zoalene 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 Zoalene as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Zoalene 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 Zoalene 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 Zoalene and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Zoalene NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Zoalene suppliers with NDC on PharmaCompass.
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