01 5Archimica S.p.A.
02 3Elementis Pharma Gmbh
03 1Fagron Inc
04 1Fuji Chemical Industries Co., Ltd.
05 1Glenmark Life Sciences Limited
06 1Kalchem International inc
07 1LETCO MEDICAL, LLC
08 1MSN Life Sciences Private Limited
09 2Medisca Inc.
10 1SNJ Labs Pvt. Ltd.
11 1Spectrum Laboratory Products Inc
12 2THINQ Pharma-CRO Limited
13 1Zhejiang Haisen Pharmaceutical Co., Ltd.
01 4SUCRALFATE
02 17Sucralfate
01 1China
02 3Germany
03 5India
04 5Italy
05 1Japan
06 1Netherlands
07 5U.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 : 55512-0020
Start Marketing Date : 2014-01-28
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 : 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 : 2024-12-31
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
A Sucralfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sucralfate, including repackagers and relabelers. The FDA regulates Sucralfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sucralfate 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 Sucralfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sucralfate supplier is an individual or a company that provides Sucralfate active pharmaceutical ingredient (API) or Sucralfate finished formulations upon request. The Sucralfate suppliers may include Sucralfate API manufacturers, exporters, distributors and traders.
click here to find a list of Sucralfate 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 Sucralfate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sucralfate 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 Sucralfate 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 Sucralfate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sucralfate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sucralfate suppliers with NDC on PharmaCompass.
We have 13 companies offering Sucralfate
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