01 1Spectrum Laboratory Products, Inc.
01 1MANGANESE GLUCONATE
01 1U.S.A
NDC Package Code : 49452-4352
Start Marketing Date : 2015-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Manganese(II) Gluconate 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 Manganese(II) Gluconate manufacturer or Manganese(II) Gluconate supplier for your needs.
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A AKOS015901565 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AKOS015901565, including repackagers and relabelers. The FDA regulates AKOS015901565 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AKOS015901565 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A AKOS015901565 supplier is an individual or a company that provides AKOS015901565 active pharmaceutical ingredient (API) or AKOS015901565 finished formulations upon request. The AKOS015901565 suppliers may include AKOS015901565 API manufacturers, exporters, distributors and traders.
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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 AKOS015901565 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for AKOS015901565 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 AKOS015901565 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 AKOS015901565 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a AKOS015901565 NDC to their finished compounded human drug products, they may choose to do so.
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