Carisoprodol Tablet
Product Images NDC 80425-0291

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Carisoprodol (NDC 80425-0291). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Pharmacy Of Tennessee, Llc, 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

Label 1 (Carisoprodol 350mg 80425 0291 01)

Carisoprodol 350 mg tablet packaging label from Advanced Rx Pharmacy of Tennessee, LLC, showing the product name, strength, dosage form, and a comparison to Soma with NDC and source NDC references. The label includes storage instructions, lot number, and expiration date details.*

FDA Label Image

Label 2 (Carisoprodol 350mg 80425 0291 02)

Carisoprodol 350 mg tablet packaging label from Advanced Rx Pharmacy of Tennessee, LLC. The label includes storage instructions (20°-25°C), a comparison to Soma, the NDC number 80425-0291, lot number placeholder, expiration date 8/31/2025, and scheduling information indicating it is a C-IV controlled substance. The label also shows source NDC 50228-0109-10 and S/N 0000000.*

FDA Label Image

Label 3 (Carisoprodol 350mg 80425 0291 03)

Carisoprodol 350 mg tablet label from Advanced Rx Pharmacy of Tennessee, LLC. The label includes storage instructions, lot number, expiration date of 8/31/2025, NDC 80425-0291, and comparison to SOMA. The product is a controlled substance classified as C-IV.*

FDA Label Image

Description (Description)

Chemical structure diagram of Carisoprodol, showing its molecular composition with atomic groups and bonds arranged according to the molecule's geometry.*

* 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.