Lithium Carbonate Tablet, Extended Release
Product Images NDC 70518-0608

3 FDA label images from Remedyrepack Inc. · 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 70518-0608). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack Inc., 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

Lithium Carbonate 300mg 70518 0608 00

Lithium Carbonate 300mg 70518 0608 00
Lithium Carbonate 300 mg extended-release tablets in a repackaged bottle form. The label shows the product strength, dosage form, and a quantity of 30 tablets. It includes manufacturer information for Rising Pharma, Inc. and repackager RemedyRepack Inc. Directions reference the package insert for use details.*
FDA Label Image

Lithium Carbonate 300mg 70518 0608 01

Lithium Carbonate 300mg 70518 0608 01
Lithium Carbonate 300 mg extended-release oral tablets, package quantity 100. The label is from RemedyRepack Inc. and notes repackaging from Rising Pharma, Inc. Directions refer to the package insert, with storage instructions at 20-25°C (68-77°F) and permitted excursions to 15-30°C (59-86°F). Contains barcode and a QR code on the label.*
FDA Label Image

Lithium Carbonate 300mg 70518 0608 02

Lithium Carbonate 300mg 70518 0608 02
Label for Lithium Carbonate 300 mg extended-release oral tablet, pack quantity 1. The label includes the NDC number 70518-0608-02 and manufacturer information for Rising Pharma, Inc. The label also shows the Remedy Repack logo and provides storage instructions and repackager details.*

* 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.