01 1Avesta Pharma Private Limited
01 1Polyethylene Glycol 6000
01 1Blank
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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PharmaCompass offers a list of Lauromacrogol 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 Lauromacrogol manufacturer or Lauromacrogol supplier for your needs.
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PharmaCompass also assists you with knowing the Lauromacrogol API Price utilized in the formulation of products. Lauromacrogol API Price is not always fixed or binding as the Lauromacrogol Price is obtained through a variety of data sources. The Lauromacrogol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A PEG 3350; ELECTROLYTES manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PEG 3350; ELECTROLYTES, including repackagers and relabelers. The FDA regulates PEG 3350; ELECTROLYTES manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PEG 3350; ELECTROLYTES 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 PEG 3350; ELECTROLYTES supplier is an individual or a company that provides PEG 3350; ELECTROLYTES active pharmaceutical ingredient (API) or PEG 3350; ELECTROLYTES finished formulations upon request. The PEG 3350; ELECTROLYTES suppliers may include PEG 3350; ELECTROLYTES API manufacturers, exporters, distributors and traders.
click here to find a list of PEG 3350; ELECTROLYTES 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 PEG 3350; ELECTROLYTES as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for PEG 3350; ELECTROLYTES 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 PEG 3350; ELECTROLYTES 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 PEG 3350; ELECTROLYTES and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a PEG 3350; ELECTROLYTES NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of PEG 3350; ELECTROLYTES suppliers with NDC on PharmaCompass.
