Levetiracetam Tablet, Film Coated
Product Images NDC 72189-229

3 FDA label images from Direct Rx · 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 Levetiracetam (NDC 72189-229). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct Rx, 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

229 (72189 0229 60)

229 (72189 0229 60)
Packaging label for LEVETIRACETAM 500 mg film-coated tablets. The label indicates a quantity of 60 tablets, distributed by Direct Rx. The label also includes generic equivalence to Keppra, lot number, expiration date, and manufacturing information from Ascend Laboratories, Inc.*
FDA Label Image

190 (72189 190 30)

190 (72189 190 30)
Packaging label for LEVETIRACETAM 250 mg film-coated tablets by DIRECT RX. The label indicates a supply of 30 tablets. It states generic equivalence to Keppra and confirms each film-coated tablet contains 250 mg of levetiracetam USP. The label includes lot number 25MA2111 and an expiration date of 10/31/22, with additional batch and manufacturing NDC codes on the right side.*
FDA Label Image

72189 190 60

72189 190 60
LEVETIRACETAM 250 mg film-coated tablets in a carton labeled for 60 tablets. The label indicates it is a generic for Keppra and is packaged and distributed by DIRECT RX, with batch and expiration details included. The label clearly states the product name, strength, dosage form, quantity, and manufacturer information.*

* 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.