Pregabalin Capsule
Product Images NDC 72189-021

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 Pregabalin (NDC 72189-021). 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

021-90 (021 90)

021-90 (021 90)
Label for PREGABALIN C-V 75 mg capsules, a human prescription drug packaged in a 90-count bottle. The label shows that each capsule contains 75 mg of pregabalin, generic for LYRICA. The product is packaged and distributed by Direct_Rx. The label includes a lot number, expiration date, NDC 72189-021-90, barcode, and cautionary statements regarding drug transfer and child safety.*
FDA Label Image

72189-021-30 (72189 021 30)

72189-021-30 (72189 021 30)
PREGABALIN C-V 75 mg oral capsules packaging label showing a count of 30 capsules. The label states it is generic for LYRICA, with each capsule containing 75 mg pregabalin. The label includes lot number SAMPLE, expiration date 8/31/24, and is distributed by Direct Rx in Dawsonville, GA.*
FDA Label Image

72189-021-60 (72189 021 60)

72189-021-60 (72189 021 60)
Packaging label of Pregabalin C-V capsules, 75 mg strength, containing 60 capsules per bottle. The label indicates it is generic for Lyrica and includes lot and expiration information for sample packaging. The labeler is Direct_Rx, with NDC 72189-021-60. The label is predominantly yellow with black text and a barcode on the side.*

* 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.