Acamprosate Calcium Tablet, Delayed Release
Product Images NDC 60687-121

4 FDA label images from American Health Packaging · 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 Acamprosate Calcium (NDC 60687-121). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

333 mg Acamprosate Calcium Tablet

333 mg Acamprosate Calcium Tablet
Acamprosate Calcium 333 mg delayed-release tablet, round and white, with imprint code 'L435' on one side and a plain opposite side. The image includes a millimeter scale for size reference. Labeler is American Health Packaging.*
FDA Label Image

Blister

Blister
Label for Acamprosate Calcium Delayed-Release Tablet 333 mg by American Health Packaging. The label shows the strength (333 mg), dosage form (delayed-release tablet), lot number, expiration date, and NDC barcode. The label is repeated three times in a vertical layout.*
FDA Label Image

Carton

Carton
Label for Acamprosate Calcium 333 mg delayed-release oral tablets by American Health Packaging. The label shows 30 tablets per package and includes storage instructions, dosage form, and barcode. It notes the drug is prescription only and provides distributor and manufacturer information.*
FDA Label Image

Structure

Structure
Chemical structure of Acamprosate Calcium shown as two acamprosate anions paired with one calcium cation (Ca2+). The structure highlights the acetamide group and sulfonate moiety in the anion.*

* 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.