Lamotrigine Tablet, Chewable
Product Images NDC 65841-689

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Lamotrigine (NDC 65841-689). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Lifesciences Limited, 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

Lamotrigine Tablets (chewable, Dispersible), 5 mglamotrigine Tablets (chewable, Dispersible), 5mg (05041788 398f 4cd7 B09d Cb709778af87 01)

Lamotrigine Tablets for Oral Suspension, USP, chewable and dispersible tablets, 5 mg strength. The label indicates a package containing 100 tablets. Manufactured by Zydus Lifesciences Limited. Includes dosage form details and usage cautions, such as verifying dispensed product, storage conditions, and instructions to keep out of reach of children.*

FDA Label Image

Lamotrigine Tablets (chewable, Dispersible), 25 mg (05041788 398f 4cd7 B09d Cb709778af87 02)

Lamotrigine Tablets for Oral Suspension, USP, 25 mg, chewable and dispersible tablets. The label indicates a package containing 100 tablets, manufactured by Zydus Lifesciences Limited. Includes dosage form and strength details, usage cautions, storage instructions, and notes on phenylketonuria. The product is Rx only and features a barcode and NDC 65841-690-01.*

FDA Label Image

Lamotrigine Tablets Usp, 25 mg (05041788 398f 4cd7 B09d Cb709778af87 03)

Packaging label for Lamotrigine Tablets, USP 25 mg oral tablets by Zydus Lifesciences Limited. The label indicates a count of 100 tablets and prescription-only status. It includes storage instructions, pharmacist caution about dispensing the Medication Guide, and a warning not to accept if the printed seal under the cap is missing or broken.*

FDA Label Image

Lamotrigine Tablets Usp, 50 mg (05041788 398f 4cd7 B09d Cb709778af87 04)

Lamotrigine Tablets USP 50 mg oral tablets label with quantity of 100 tablets. The label includes the caution to verify product dispense and instructions for pharmacists to dispense the Medication Guide with each prescription. It displays storage conditions, warnings, and manufacturer information for Zydus Lifesciences Limited, India.*

FDA Label Image

Lamotrigine Tablets Usp, 100 mg (05041788 398f 4cd7 B09d Cb709778af87 05)

Lamotrigine Tablets, USP 100 mg oral tablets packaging label from Zydus Lifesciences Limited. The label indicates 100 tablets per container with an Rx only designation. The label includes storage instructions, a warning to pharmacists to dispense the Medication Guide, and a caution to verify the product dispensed. The NDC number 65841-684-01 is displayed.*

FDA Label Image

Lamotrigine Tablets Usp, 150 mg (05041788 398f 4cd7 B09d Cb709778af87 06)

Lamotrigine Tablets USP 150 mg oral tablets label. The packaging shows the product name, strength, and form, with a count of 60 tablets. It is labeled for prescription use only and manufactured by Zydus Lifesciences Limited in India. The label includes storage instructions, a caution to verify the product dispensed, and a note to dispense the accompanying medication guide.*

FDA Label Image

Lamotrigine Tablets Usp, 200 mg (05041788 398f 4cd7 B09d Cb709778af87 07)

Lamotrigine Tablets USP 200 mg oral tablets packaging label from Zydus Lifesciences Limited. The label indicates a 60-tablet count with a caution to verify product dispensed and instructions for pharmacists to dispense the medication guide. Storage instructions and manufacturing origin (India) are also present.*

FDA Label Image

Lamotrigine Tablets Usp, 250 mg (05041788 398f 4cd7 B09d Cb709778af87 08)

Lamotrigine Tablets USP 250 mg oral tablet label with packaging details. The label states the dosage strength of 250 mg and the package contains 500 tablets. It includes cautionary notes for pharmacists and storage instructions. The labeler is Zydus Lifesciences Limited and manufacturing is by Cadila Healthcare Ltd, India. The NDC is 65841-687-05.*

* 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.