01 1Allsino Pharmaceutical Co., Ltd.
02 2Apothecon Pharmaceuticals Pvt Ltd
03 1Maithri Laboratories Private Limited
04 1Micro Labs Limited
05 1Qingdao Biopeptek Co., Ltd.
06 1Qingdao Qinzeyuan Biotechnology Co., Ltd
01 1SALCAPROZATE SODIUM
02 5Salcaprozate Sodium
03 1Salcaprozate sodium
01 4India
02 1U.S.A
03 2Blank
NDC Package Code : 76339-179
Start Marketing Date : 2022-11-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (19.999kg/19.999kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 76339-505
Start Marketing Date : 2023-11-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (19.999kg/19.999kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 73212-066
Start Marketing Date : 2023-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42571-541
Start Marketing Date : 2025-06-12
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (10kg/10kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71666-012
Start Marketing Date : 2021-03-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 84536-378
Start Marketing Date : 2025-01-20
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
NDC Package Code : 85512-2037
Start Marketing Date : 2025-06-02
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
12
PharmaCompass offers a list of Salcaprozate Sodium 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 Salcaprozate Sodium manufacturer or Salcaprozate Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Salcaprozate Sodium API Price utilized in the formulation of products. Salcaprozate Sodium API Price is not always fixed or binding as the Salcaprozate Sodium Price is obtained through a variety of data sources. The Salcaprozate Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 203787-91-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 203787-91-1, including repackagers and relabelers. The FDA regulates 203787-91-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 203787-91-1 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 203787-91-1 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 203787-91-1 supplier is an individual or a company that provides 203787-91-1 active pharmaceutical ingredient (API) or 203787-91-1 finished formulations upon request. The 203787-91-1 suppliers may include 203787-91-1 API manufacturers, exporters, distributors and traders.
click here to find a list of 203787-91-1 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 203787-91-1 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for 203787-91-1 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 203787-91-1 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 203787-91-1 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 203787-91-1 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of 203787-91-1 suppliers with NDC on PharmaCompass.
We have 4 companies offering 203787-91-1
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