01 1Jost Chemical Co.
02 1Macco Organiques, S.R.O.
03 1Professional Compounding Centers of America dba PCCA
01 1ZINC SULFATE
02 1ZINC SULFATE MONOHYDRATE
03 1Zinc Sulfate Monohydrate
01 1Canada
02 1U.S.A
03 1United Kingdom
NDC Package Code : 55570-540
Start Marketing Date : 2015-02-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 67706-0007
Start Marketing Date : 2015-02-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-1364
Start Marketing Date : 2002-07-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
A Zinc Sulfate Monohydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zinc Sulfate Monohydrate, including repackagers and relabelers. The FDA regulates Zinc Sulfate Monohydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zinc Sulfate Monohydrate 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 Sulfate Monohydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zinc Sulfate Monohydrate supplier is an individual or a company that provides Zinc Sulfate Monohydrate active pharmaceutical ingredient (API) or Zinc Sulfate Monohydrate finished formulations upon request. The Zinc Sulfate Monohydrate suppliers may include Zinc Sulfate Monohydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Zinc Sulfate Monohydrate 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 Sulfate Monohydrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Zinc Sulfate Monohydrate 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 Sulfate Monohydrate 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 Sulfate Monohydrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Zinc Sulfate Monohydrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Zinc Sulfate Monohydrate suppliers with NDC on PharmaCompass.
We have 3 companies offering Zinc Sulfate Monohydrate
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