Sucralfate Suspension
Product Images NDC 81033-149
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sucralfate (NDC 81033-149). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Kesin Pharma Corporation, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Kesin Pharma Logo (Kesin Logo)
Sucralfate 40 Count Carton (Sucra Os 10ml Carton 40ct)
This is a description of Sucralfate Oral Suspension, with 1g per 10 mL concentration. The product is delivered in 10 mL unit dose cups, with a NDC code of 81033-149-44. It is intended for institutional use only and should be stored at temperatures between 68°F to 77°F (20°C to 25°C). The expiration date is indicated as 00-MAY-0000 with LOT number K0000000. The product is packaged and distributed by Kesin Pharma Corporation in Oldsmar, Florida. For further information, refer to the insert provided.*
Sucralfate 100 Count Case (Sucra Os 10ml Case 2x50ct)
This text is a label for Sucralfate Oral Suspension containing 1 g per 10 mL. Each case delivers 10 mL and contains 100 UD cups. The product should be stored between 68°F to 77°F (20°C to 25°C). The expiration date is indicated as 00-JUN-0000 with LOT: KOO00000. The label also includes various numerical codes and mentions internal use only. The product is packaged and distributed by Kesin Pharma Corporation in Oldsmar, FL.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.