01 1Avesta Pharma Private Limited
01 1Polyethylene Glycol 6000
01 1India
NDC Package Code : 57449-011
Start Marketing Date : 2023-05-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A Polyethylene Glycol 6000 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Polyethylene Glycol 6000, including repackagers and relabelers. The FDA regulates Polyethylene Glycol 6000 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Polyethylene Glycol 6000 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 Polyethylene Glycol 6000 supplier is an individual or a company that provides Polyethylene Glycol 6000 active pharmaceutical ingredient (API) or Polyethylene Glycol 6000 finished formulations upon request. The Polyethylene Glycol 6000 suppliers may include Polyethylene Glycol 6000 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 Polyethylene Glycol 6000 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Polyethylene Glycol 6000 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 Polyethylene Glycol 6000 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 Polyethylene Glycol 6000 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Polyethylene Glycol 6000 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Polyethylene Glycol 6000 suppliers with NDC on PharmaCompass.
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