Ferrous Sulfate
Product Images NDC 76413-308

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Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Ferrous Sulfate (NDC 76413-308). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Central Texas Community Health Centers, 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

Principal Display Panel (325 MG Tablet Bottle Label)

Principal Display Panel (325 MG Tablet Bottle Label)
This is a prescription label for Ferrous Sulfate tablets, 325mg strength, with instructions to take 1 to 3 tablets per day with food, as directed. The medication is supplied in a bottle containing 100 tablets, with the expiration date mentioned as 1/1/01. The drug is manufactured by Sun Pharma, and the label contains the National Drug Code (NDC) as 76413-308-01. The text warns that Federal law prohibits the transfer of this medicine to anyone other than the person for whom it is prescribed.*

* 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.