Lithium Carbonate Capsule
Product Images NDC 68462-222

5 FDA label images from Glenmark Pharmaceuticals Inc., Usa · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Lithium Carbonate (NDC 68462-222). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Glenmark Pharmaceuticals Inc., Usa, 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

Logo1 (Logo1)

FDA Label Image

Logo2 (Logo2)

FDA Label Image

Label150mg100s (Label150mg100s)

Label150mg100s (Label150mg100s)
Lithium Carbonate Capsules USP 150 mg oral capsules label from Glenmark Pharmaceuticals Inc., USA. The label states the package contains 100 capsules, with storage instructions, dosage information, and a barcode. It includes the NDC 68462-220-01 and a note to dispense the medication guide with the product.*
FDA Label Image

Label300mg100s (Label300mg100s)

Label300mg100s (Label300mg100s)
Lithium Carbonate Capsules USP 300 mg packaging label showing 100 capsules in the container. The label includes the National Drug Code (NDC) 68462-221-01 and indicates the product is by Glenmark Pharmaceuticals Inc., USA. The label features usage and storage instructions, a reminder to dispense the Medication Guide, and contact information for Glenmark Pharmaceuticals.*
FDA Label Image

Label600mg100s (Label600mg100s)

Label600mg100s (Label600mg100s)
Lithium Carbonate Capsules USP 600 mg label from Glenmark Pharmaceuticals Inc., USA. The label indicates the product is prescription-only, contains 100 capsules, and provides dosing and storage instructions along with manufacturer contact information and barcodes.*

* 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.