Cefadroxil Capsule
Product Images NDC 80425-0432

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Cefadroxil (NDC 80425-0432). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Of Tennessee, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Cefadroxil 50mg Capsule #10 (Cefadroxil 500mg 80425 0432 01)

Label for Cefadroxil 500 mg capsule by Advanced Rx of Tennessee, LLC. The label includes NDC 80425-0432-01 and lot and expiration date fields (3/31/2027). It also references comparison to Duricef with related NDC and source numbers. Storage instructions are provided (20° to 25°C).*

FDA Label Image

Cefadroxil 50mg Capsule #20 (Cefadroxil 500mg 80425 0432 02)

Label for Cefadroxil 500 mg capsules by Advanced Rx of Tennessee, LLC, Nashville. The label includes NDC 80425-0432, storage instructions at 20°-25°C (68°-77°F), and expiration date 3/31/2027. It notes comparison to Duricef and is marked for prescription use only.*

FDA Label Image

Cefadroxil 50mg Capsule #30 (Cefadroxil 500mg 80425 0432 03)

Label for Cefadroxil 500 mg capsule by Advanced Rx of Tennessee, LLC. The packaging includes NDC 80425-0432-03, lot and expiration date information, and notes comparison to Duricef. Label also displays storage instructions and a barcode, indicating prescription use only.*

FDA Label Image

Molecular Structure (Cefadroxilcapsules Figure 01)

Chemical structure of cefadroxil, an antibiotic represented by a beta-lactam ring fused to a dihydrothiazine ring, with specific functional groups including an amino group and a carboxyl group, depicted with molecular bonds and water of hydration indicated.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.