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Sucralfate Raw Medication for Active Duodenal Ulcers Treatment

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  • Specifications

Buy USP Sucralfate Raw Medication for Active Duodenal Ulcers Treatment Online CAS 54182-58-0

 

Sucralfate Specification

Product Name: Sucralfate
CAS: 54182-58-0
Standard: USP
Level: Pharmaceutical grade
Appearance: white powder
Packing: 25KG/cardboard drum
Ingredients: Basic aluminium salt of sucrose sulphate. According to the calculation of dry goods, aluminum (Al) should be 15.5% to 18.5%, the total content of 30-38% tax rebate rate of 13%
Physicochemical properties: white or almost white powder; odorless, almost odorless; This product is almost insoluble in water, ethanol or chloroform; soluble in dilute hydrochloric acid or dilute sulfuric acid, slightly soluble in dilute nitric acid.
Category: Pharmaceutical Raw Materials
Field: Antacids
Deferred Products: (1) Sucralfate Oral Suspensions (2) Sucralfate Dispersible Tablets (3) Sucralfate Chewable Tablets (4) Sucralfate Capsules
Use: For the treatment of gastric ulcer, duodenal ulcer and gastritis.
Usage and dosage: 1. Active gastric and duodenal ulcers: 1g each time, 3 to 4 times a day, medication for 4 to 6 weeks. 2. Prevention of recurrent duodenal ulcers: 1g each time, 2 times a day.

 

What is Sucralfate?

Sucralfate is a medication primarily taken to treat active duodenal ulcers. Sucralfate is also used for the treatment of gastroesophageal reflux disease (GERD) and stress ulcers.

Sucralfate is a sucrose sulfate-aluminium complex that binds to the ulcer, creating a physical barrier that protects the gastrointestinal tract from stomach acid and prevents the degradation of mucus. It also promotes bicarbonate production and acts like an acid buffer with cytoprotective properties.

 

Sucralfate certificate of Analysis

Product name Sucralfate
CAS No. 54182-58-0 Outer Packing 25kg / drum
Production date 2017.04.04 Shelf life 2020.04.03
Standard adopted USP
Items of analysis Specification Results
Clarity and color of solution The solution is clear and practically colorless The solution is clear
Identification 1.The retention time of the peak correspond to standard;(2)(3)Positive Conform
Chloride ≤0.5% <0.5%
Arsenic ≤0.0004% <0.0004%
Heavy metals ≤0.002% <0.002%
Limit of pyridine and 2-methylpyridine ≤0.05% <0.05%
Limit of sucrose heptasulfate Meets the requirements Conform
Aluminum content 15.5% ~ 18.5% 17.8%
Acid neutralization equivalent ≥12mEq 15.6mEq
Assay 30% ~ 38% 31.4%
Conclusion Qualified

 

Sucralfate Side Effects

Constipation, dry mouth, upset stomach, gas, and nausea may occur. If any of these effects persist or worsen, notify your doctor or pharmacist promptly.

 

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