01 5Archimica S.p.A.
02 3Elementis Pharma Gmbh
03 1Fagron Inc
04 1Fuji Chemical Industries Co., Ltd.
05 1Glenmark Life Sciences Limited
06 1Gulbrandsen Technologies India Private Limited
07 1Kalchem International inc
08 1LETCO MEDICAL, LLC
09 1MSN Life Sciences Private Limited
10 2Medisca Inc.
11 1SNJ Labs Pvt. Ltd.
12 1Spectrum Laboratory Products Inc
13 2THINQ Pharma-CRO Limited
14 1Zhejiang Haisen Pharmaceutical Co., Ltd.
01 5SUCRALFATE
02 17Sucralfate
01 1China
02 3Germany
03 5India
04 5Italy
05 1Japan
06 1Netherlands
07 6U.S.A
NDC Package Code : 55512-0002
Start Marketing Date : 2009-07-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 55512-0009
Start Marketing Date : 2009-09-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 55512-0019
Start Marketing Date : 2012-09-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-0039
Start Marketing Date : 1998-04-01
End Marketing Date : 2026-03-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 31260-401
Start Marketing Date : 2025-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0318
Start Marketing Date : 2012-04-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-3219
Start Marketing Date : 2020-09-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-7401
Start Marketing Date : 1998-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54469-0009
Start Marketing Date : 2023-09-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54469-0010
Start Marketing Date : 2023-11-07
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 Sucralfate 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 Sucralfate manufacturer or Sucralfate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sucralfate manufacturer or Sucralfate supplier.
PharmaCompass also assists you with knowing the Sucralfate API Price utilized in the formulation of products. Sucralfate API Price is not always fixed or binding as the Sucralfate Price is obtained through a variety of data sources. The Sucralfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ulsanic manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ulsanic, including repackagers and relabelers. The FDA regulates Ulsanic manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ulsanic 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 Ulsanic manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ulsanic supplier is an individual or a company that provides Ulsanic active pharmaceutical ingredient (API) or Ulsanic finished formulations upon request. The Ulsanic suppliers may include Ulsanic API manufacturers, exporters, distributors and traders.
click here to find a list of Ulsanic 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 Ulsanic as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ulsanic 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 Ulsanic 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 Ulsanic and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ulsanic NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ulsanic suppliers with NDC on PharmaCompass.
We have 14 companies offering Ulsanic
Get in contact with the supplier of your choice:
