Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
01 1Ofichem BV
02 1AURORIUM LLC
03 1Global Calcium Private Limited
01 1Zinc Acetate
02 1Zinc Acetate Dihydrate
03 1Zinc Acetate Dihydrate Milled
01 1India
02 1Netherlands
03 1U.S.A
Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
NDC Package Code : 62675-1444
Start Marketing Date : 2018-07-02
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 25441-0080
Start Marketing Date : 2015-12-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 64162-0219
Start Marketing Date : 2023-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
A Zinc Acetate Dihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zinc Acetate Dihydrate, including repackagers and relabelers. The FDA regulates Zinc Acetate Dihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zinc Acetate Dihydrate 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 Acetate Dihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zinc Acetate Dihydrate supplier is an individual or a company that provides Zinc Acetate Dihydrate active pharmaceutical ingredient (API) or Zinc Acetate Dihydrate finished formulations upon request. The Zinc Acetate Dihydrate suppliers may include Zinc Acetate Dihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Zinc Acetate Dihydrate 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 Acetate Dihydrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Zinc Acetate Dihydrate 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 Acetate Dihydrate 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 Acetate Dihydrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Zinc Acetate Dihydrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Zinc Acetate Dihydrate suppliers with NDC on PharmaCompass.
We have 3 companies offering Zinc Acetate Dihydrate
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