Tramadol Hydrochloride Tablet, Coated
Product Images NDC 72189-311

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Tramadol Hydrochloride (NDC 72189-311). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Directrx, 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

Fhtyfgh (72189 311 12)

Tramadol HCL C-IV 50 mg coated tablets by DirectRx, labeled as generic for Ultram with a package containing 12 tablets. The yellow and white label includes dosage strength 50 mg and indicates the product type as a human prescription drug with oral route administration.*

FDA Label Image

Yhght (72189 311 60)

Tramadol HCL C-IV 50 mg coated oral tablets, packaged in a container of 60 tablets. The label identifies the product as Tramadol Hydrochloride, 50 mg strength, produced by DirectRx. It includes lot number and expiration date information, with visible NDC codes.*

FDA Label Image

Yhght (72189 311 72)

Tramadol HCL C-IV 50 mg coated tablets, 120 count, packaged and distributed by DirectRx. The label highlights the generic name Ultram and states each tablet contains Tramadol Hydrochloride USP 50 mg. Additional text includes lot number, discard after date, and packaging details.*

FDA Label Image

Yhght (72189 311 90)

Tramadol HCL C-IV 50 mg coated tablets, 90 count bottle label. The label indicates the product is generic for Ultram, contains 50 mg Tramadol Hydrochloride USP per film-coated tablet, and is packaged and distributed by DirectRx. Additional details include lot number, expiration date, and manufacturer information from Dawsonville, GA.*

* 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.