Salsalate
Product Images NDC 13273-209

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Salsalate (NDC 13273-209). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Andapharm 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

Chemical Structure (Salsalate 01)

Chemical structure of the active ingredient shown, comprising two benzene rings linked by an ester group with carboxyl and hydroxyl substituents, consistent with salsalate's molecular structure.*

FDA Label Image

Principal Display Panel (500 mg Tablet Bottle Label)

Salsalate Tablets USP 500 mg bottle label by ANDAPharm LLC. The label indicates the product contains 100 film-coated tablets, prescription only, with usage and storage instructions. It includes the NDC number 13273-209-03 and safety warnings to keep out of reach of children.*

FDA Label Image

Principal Display Panel (750 mg Tablet Bottle Label)

Label for Salsalate Tablets USP 750 mg by ANDAPharm LLC. The label indicates the product is Rx only, contains 100 tablets, and includes dosage and storage instructions. Manufactured by ANDAPharm LLC, Fort Lauderdale, FL 33309, with NDC 13273-210-03.*

* 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.