01 2Fagron Inc
01 2Cellulose Microcrystalline
01 2Netherlands
NDC Package Code : 51552-0548
Start Marketing Date : 2004-01-02
End Marketing Date : 2027-02-15
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51552-1528
Start Marketing Date : 2018-12-11
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
A Cellulose, microcrystalline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cellulose, microcrystalline, including repackagers and relabelers. The FDA regulates Cellulose, microcrystalline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cellulose, microcrystalline API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Cellulose, microcrystalline supplier is an individual or a company that provides Cellulose, microcrystalline active pharmaceutical ingredient (API) or Cellulose, microcrystalline finished formulations upon request. The Cellulose, microcrystalline suppliers may include Cellulose, microcrystalline API manufacturers, exporters, distributors and traders.
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 Cellulose, microcrystalline as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cellulose, microcrystalline 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 Cellulose, microcrystalline 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 Cellulose, microcrystalline and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cellulose, microcrystalline NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cellulose, microcrystalline suppliers with NDC on PharmaCompass.
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