Tramadol Hydrochloride
Product Images NDC 61919-892

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Tramadol Hydrochloride (NDC 61919-892). 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

5971

5971
Packaging label for TRAMADOL HCL C-IV 50mg oral tablets, 240 count, labeled as generic for Ultram. The label includes the lot number SAMPLE, expiration date 1/31/23, and is packaged and distributed by DirectRX. The label also contains federal caution information and storage instructions.*
FDA Label Image

5972

5972
Label for TRAMADOL HCL C-IV, 50 mg, showing 240 tablets. The label includes information that each tablet contains tramadol hydrochloride USP 50 mg. It is distributed by DirectRx and lists lot number SAMPLE and expiration date 1/31/23. The label also contains regulatory warnings and a barcode.*
FDA Label Image

5973

5973
Label for TRAMADOL HCL C-IV extended-release tablets, 50 mg strength, containing 90 tablets per bottle. The label states it is a generic for Ultram and includes cautions and distribution information by DirectRX. The label shows lot number SAMPLE and expiration date 1/31/23.*
FDA Label Image

5974

5974
Label of TRAMADOL HCL C-IV 50mg tablets, 60 count, generic for Ultram, containing tramadol hydrochloride USP 50mg per tablet. Packaged and distributed by DirectRx. Includes NDC 61919-597-60 and lot number SAMPLE with discard date 1/31/23. Additional small repeating labels on the right side with the same drug and lot information.*
FDA Label Image

5975

5975
Label for TRAMADOL HCL C-IV tablets, 50 mg strength, containing 40 tablets per package. The label indicates the generic name as tramadol hydrochloride USP 50 mg. It is labeled as a product of DirectRx and includes regulatory and packaging information, such as lot number SAMPLE and discard date 1/31/23. The label also states it is generic for ULTRAM.*
FDA Label Image

5976

5976
Label for TRAMADOL HCL C-IV 50mg tablets, 30 count, generic for Ultram. The label includes dosage strength, quantity, and mentions tramadol hydrochloride USP 50mg per tablet. It shows the NDC number 61919-597-30 and is packaged and distributed by DirectRx in Dawsonville, GA. Additional information includes lot number SAMPLE and discard date 1/31/23.*
FDA Label Image

5977

5977
Packaging label for Tramadol HCL C-IV 50mg extended-release tablets. The label shows a count of 20 tablets, marked as generic for Ultram, with each tablet containing 50mg tramadol hydrochloride. The product is packaged and distributed by DirectRX, with a lot number SAMPLE and expiration date 1/31/23. Additional NDC and manufacturer information is noted on the right side panel.*
FDA Label Image

5978

5978
Label for TRAMADOL HYDROCHLORIDE ER 50mg tablets, 180 count, distributed by DirectRX. The label specifies the product as a generic for ULTRAM and includes details such as NDC 61919-597-82, lot SAMPLE, and an expiration date of 1/31/23. Packaging originates from Dawsonville, GA.*
FDA Label Image

892 (892 60)

892 (892 60)
TRAMADOL HYDROCHLORIDE ER 100 mg extended-release tablets, 60 count carton, labeled as generic for Ultram ER. The label shows the strength (100 mg), quantity (60 tablets), and includes warnings about dizziness, nausea, headache, dry mouth, and diarrhea. Packaged and distributed by DirectRX in Alpharetta, 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.