01 1Osauhing TBD Pharmatech
01 1Physostigmine Salicylate
01 1Estonia
NDC Package Code : 83030-377
Start Marketing Date : 2022-10-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100g/100g)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Physostigmine Salicylate 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 Physostigmine Salicylate manufacturer or Physostigmine Salicylate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Physostigmine Salicylate manufacturer or Physostigmine Salicylate supplier.
PharmaCompass also assists you with knowing the Physostigmine Salicylate API Price utilized in the formulation of products. Physostigmine Salicylate API Price is not always fixed or binding as the Physostigmine Salicylate Price is obtained through a variety of data sources. The Physostigmine Salicylate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Physostigmine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Physostigmine, including repackagers and relabelers. The FDA regulates Physostigmine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Physostigmine 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 Physostigmine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Physostigmine supplier is an individual or a company that provides Physostigmine active pharmaceutical ingredient (API) or Physostigmine finished formulations upon request. The Physostigmine suppliers may include Physostigmine API manufacturers, exporters, distributors and traders.
click here to find a list of Physostigmine 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 Physostigmine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Physostigmine 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 Physostigmine 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 Physostigmine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Physostigmine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Physostigmine suppliers with NDC on PharmaCompass.
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