SPI Pharma has been solving formulation challenges using superior functional materials.
01 2SPI Pharma, Inc.
02 1Elementis Pharma Gmbh
03 1Professional Compounding Centers of America
01 2ALUMINUM HYDROXIDE
02 1Aluminum Hydroxide Magnesium Carbonate
03 1Dried Aluminum Hydroxide Sorbitol Blend
01 1Germany
02 2U.S.A
03 1United Kingdom
SPI Pharma has been solving formulation challenges using superior functional materials.
ALUMINUM HYDROXIDE; CARBONATE ION; MAGNESIUM CARBONATE
NDC Package Code : 12784-420
Start Marketing Date : 2014-11-18
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (53kg/100kg 4.31/100kg 26kg/100kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
SPI Pharma has been solving formulation challenges using superior functional materials.
ALUMINUM HYDROXIDE; CARBON DIOXIDE
NDC Package Code : 12784-442
Start Marketing Date : 2019-12-09
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (61.5kg/100kg 5kg/100kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 55603-211
Start Marketing Date : 2010-09-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-5167
Start Marketing Date : 2022-05-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
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PharmaCompass offers a list of Aluminium Hydroxide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Aluminium Hydroxide manufacturer or Aluminium Hydroxide supplier for your needs.
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PharmaCompass also assists you with knowing the Aluminium Hydroxide API Price utilized in the formulation of products. Aluminium Hydroxide API Price is not always fixed or binding as the Aluminium Hydroxide Price is obtained through a variety of data sources. The Aluminium Hydroxide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Aluminium Hydroxide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aluminium Hydroxide, including repackagers and relabelers. The FDA regulates Aluminium Hydroxide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aluminium Hydroxide 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 Aluminium Hydroxide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aluminium Hydroxide supplier is an individual or a company that provides Aluminium Hydroxide active pharmaceutical ingredient (API) or Aluminium Hydroxide finished formulations upon request. The Aluminium Hydroxide suppliers may include Aluminium Hydroxide API manufacturers, exporters, distributors and traders.
click here to find a list of Aluminium Hydroxide 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 Aluminium Hydroxide as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Aluminium Hydroxide 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 Aluminium Hydroxide 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 Aluminium Hydroxide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Aluminium Hydroxide NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Aluminium Hydroxide suppliers with NDC on PharmaCompass.
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