Amoxicillin Powder, For Suspension
Product Images NDC 0143-9889
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Amoxicillin (NDC 0143-9889). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Hikma Pharmaceuticals Usa Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Amoxicillin For Oral Suspension Usp, 125 mg/5 mL (100 mL When Reconstituted) Bottle Label Image (Amoxicillin For Oral Suspension 125 mg And 250 mg 2)
This text provides information on amoxicillin oral suspension with a concentration of 125 mg/5 mL. It includes instructions for dosage for adults and children, as well as reconstitution guidelines. The medication should be stored at room temperature between 20°C to 25°C and discarded after 14 days. The manufacturer is Hikma Pharmaceuticals, and the product is not for injection.*
Amoxicillin For Oral Suspension Usp, 250 mg/5 mL (100 mL When Reconstituted) Bottle Label Image (Amoxicillin For Oral Suspension 125 mg And 250 mg 3)
This text provides detailed instructions for reconstituting and dosing amoxicillin oral suspension, which is used to treat bacterial infections. The usual adult dosage is 250 to 500 mg every 8 hours, while the child dosage depends on age, weight, and infection severity. The powder should be stored at room temperature and discarded after 14 days. The medication is not for injection and should be kept out of reach of children. The product details include the manufacturer's information and National Drug Code (NDC) number.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.