01 15N Plus Lubeck GmbH
02 1Par Active Technologies Private Limited
03 1Union Quimico Farmaceutica SA
01 3Bismuth Subcitrate Potassium
01 1Canada
02 1Spain
03 1U.S.A
NDC Package Code : 47167-7777
Start Marketing Date : 2022-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 70054-036
Start Marketing Date : 2023-03-07
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (16kg/16kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49711-1521
Start Marketing Date : 2024-09-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Bismuth Subcitrate 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 Bismuth Subcitrate Potassium manufacturer or Bismuth Subcitrate Potassium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Bismuth Subcitrate Potassium manufacturer or Bismuth Subcitrate Potassium supplier.
PharmaCompass also assists you with knowing the Bismuth Subcitrate Potassium API Price utilized in the formulation of products. Bismuth Subcitrate Potassium API Price is not always fixed or binding as the Bismuth Subcitrate Potassium Price is obtained through a variety of data sources. The Bismuth Subcitrate Potassium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A PYLERA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PYLERA, including repackagers and relabelers. The FDA regulates PYLERA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PYLERA 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 PYLERA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A PYLERA supplier is an individual or a company that provides PYLERA active pharmaceutical ingredient (API) or PYLERA finished formulations upon request. The PYLERA suppliers may include PYLERA API manufacturers, exporters, distributors and traders.
click here to find a list of PYLERA 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 PYLERA as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for PYLERA 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 PYLERA 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 PYLERA and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a PYLERA NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of PYLERA suppliers with NDC on PharmaCompass.
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