01 13Elementis SRL, Inc.
02 11Gulbrandsen Technologies India Private Limited
03 4The Procter & Gamble Manufacturing Company
01 1ALUMINUM SESQUICHLOROHYDRATE WITH CALCIUM CHLORIDE AND GLYCINE
02 2ALUMINUM ZIRCONIUM TETRACHLOROHYDREX
03 1ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
04 4ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLYCINE
05 2ALUMINUM ZIRCONIUM TRICHLOROHYDREX
06 1ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
07 2Aluminum Zirconium Pentachlorohydrex Gly
08 9Aluminum Zirconium Tetrachlorohydrex Gly
09 1Aluminum Zirconium Trichlorodyrex Gly
10 5Aluminum Zirconium Trichlorohydrex Gly
01 13Germany
02 15U.S.A
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
NDC Package Code : 31260-204
Start Marketing Date : 2006-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
NDC Package Code : 31260-210
Start Marketing Date : 2010-12-09
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
NDC Package Code : 31260-206
Start Marketing Date : 2006-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
NDC Package Code : 31260-213
Start Marketing Date : 2010-12-16
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
NDC Package Code : 31260-208
Start Marketing Date : 2019-09-08
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
NDC Package Code : 31260-214
Start Marketing Date : 2014-02-14
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
NDC Package Code : 31260-221
Start Marketing Date : 2014-11-24
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
NDC Package Code : 31260-217
Start Marketing Date : 2018-05-08
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
NDC Package Code : 31260-222
Start Marketing Date : 2023-07-16
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
NDC Package Code : 31260-218
Start Marketing Date : 2009-07-23
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Zirconium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zirconium, including repackagers and relabelers. The FDA regulates Zirconium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zirconium 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 Zirconium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zirconium supplier is an individual or a company that provides Zirconium active pharmaceutical ingredient (API) or Zirconium finished formulations upon request. The Zirconium suppliers may include Zirconium API manufacturers, exporters, distributors and traders.
click here to find a list of Zirconium 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 Zirconium as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Zirconium 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 Zirconium 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 Zirconium and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Zirconium NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Zirconium suppliers with NDC on PharmaCompass.
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