Lithium Carbonate Tablet, Extended Release
Product Images NDC 68084-655

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 Lithium Carbonate (NDC 68084-655). 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

450 mg Lithium Carbonate Er Tablet

450 mg Lithium Carbonate Er Tablet
Lithium Carbonate 450 mg extended-release tablet shown from front and back. The white, round tablet is embossed with the numbers '54' above '346' on the front side and has a single score line on the back side. A millimeter scale is visible along the sides for size reference.*
FDA Label Image

Blister

Blister
Lithium Carbonate Extended-release Tablet USP 450 mg packaging label. The label shows the product name, dosage strength, dosage form as extended-release tablet, a barcode, expiration and lot number placeholders, and the labeler American Health Packaging, Columbus, Ohio 43217. This is a multi-instance sheet of identical labels for the oral prescription drug.*
FDA Label Image

Carton

Carton
Lithium Carbonate Extended-release Tablets USP, 450 mg, in a package of 100 tablets (10 x 10). The label displays the NDC 68084-655-01 and indicates the product is Rx only. Manufacturer is American Health Packaging. The label includes dosage, storage instructions, and warnings to keep out of reach of children.*

* 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.