01 3Cytec Industries Inc.
01 3Docusate Sodium
01 3Belgium
NDC Package Code : 60378-100
Start Marketing Date : 2001-01-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 60378-050
Start Marketing Date : 2001-01-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (0.5kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 60378-085
Start Marketing Date : 2001-01-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (0.85kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
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PharmaCompass offers a list of Docusate Potassium 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 Docusate Potassium manufacturer or Docusate Potassium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Docusate Potassium manufacturer or Docusate Potassium supplier.
PharmaCompass also assists you with knowing the Docusate Potassium API Price utilized in the formulation of products. Docusate Potassium API Price is not always fixed or binding as the Docusate Potassium Price is obtained through a variety of data sources. The Docusate Potassium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MICRO-ENEMA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MICRO-ENEMA, including repackagers and relabelers. The FDA regulates MICRO-ENEMA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MICRO-ENEMA 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 MICRO-ENEMA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A MICRO-ENEMA supplier is an individual or a company that provides MICRO-ENEMA active pharmaceutical ingredient (API) or MICRO-ENEMA finished formulations upon request. The MICRO-ENEMA suppliers may include MICRO-ENEMA API manufacturers, exporters, distributors and traders.
click here to find a list of MICRO-ENEMA 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 MICRO-ENEMA as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for MICRO-ENEMA 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 MICRO-ENEMA 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 MICRO-ENEMA and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a MICRO-ENEMA NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of MICRO-ENEMA suppliers with NDC on PharmaCompass.
