Tramadol Hydrochloride Tablet, Coated
Product Images NDC 80425-0501

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Tramadol Hydrochloride (NDC 80425-0501). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx 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

Tramadol HCl 50mg #15 (Tramadol HCl 50mg 80425 0501 01)

Label of Tramadol Hydrochloride 50 mg coated tablets, packaged by Advanced Rx of Tennessee, LLC in Nashville, TN. The label includes a barcode, lot number placeholder, expiration date of 1/31/2027, and notes it is a C-IV controlled substance for prescription use only. It references to compare to ULTRAM and provides storage instructions between 20-25°C (68-77°F).*

FDA Label Image

Tramadol HCl 50mg # 30 (Tramadol HCl 50mg 80425 0501 02)

Tramadol Hydrochloride 50 mg coated tablets packaging label, showing the product name and strength prominently. The label indicates prescription-only status (C-IV) and includes lot and expiration date information. It lists Advanced Rx of Tennessee, LLC as the packer and Amneal Pharmace as the pharmacy. The label also contains storage instructions and cautions against transferring the drug to others.*

FDA Label Image

Tramadol HCl 50mg #6 0 (Tramadol HCl 50mg 80425 0501 03)

Packaging label for Tramadol Hydrochloride 50 mg coated tablets by Advanced Rx of Tennessee, LLC. The label includes the product name, strength, dosage form, NDC number (80425-0501-03), regulatory class (C-IV), and storage instructions. It also shows a barcode and prescription-only status. The package count is 60 tablets.*

FDA Label Image

Tramadol HCl 50mg #90 (Tramadol HCl 50mg 80425 0501 04)

Tramadol Hydrochloride 50 mg coated tablet packaging label. The label shows the product name, strength, dosage form, and contains storage instructions (store at 20-25°C). It includes the labeler name AdvancedRx Nashville TN, lot number, expiration date, NDC 80425-0501-04, and C-IV controlled substance designation with Rx only restriction. Barcodes and a comparison to Ultram are also visible.*

FDA Label Image

Tramadol HCl 50mg #120 (Tramadol HCl 50mg 80425 0501 05)

Tramadol Hydrochloride 50 mg coated tablet label from Advanced Rx of Tennessee, LLC. The label includes NDC 80425-0501-05, dosage form as tablet, and storage instructions at 20°-25°C (68°-77°F). It is marked as Schedule IV (C-IV) prescription only. The label also references comparison to Ultram and lists expiration date 1/31/2027.*

FDA Label Image

Tramadol HCl 50mg #40 (Tramadol HCl 50mg 80425 0501 06)

Tramadol Hydrochloride 50 mg coated tablet label from Advanced Rx of Tennessee, LLC. The label includes storage temperature instructions, lot number, expiration date 1/31/2027, and indicates prescription use only (C-IV). It refers to comparison to Ultram and includes labeler and NDC numbers.*

FDA Label Image

Tramadol HCl 50mg #180 (Tramadol HCl 50mg 80425 0501 07)

Label for Tramadol Hydrochloride 50 mg coated tablets, manufactured by Advanced Rx of Tennessee, LLC. The label includes storage instructions (20°-25°C), controlled substance classification (C-IV), prescription status (Rx Only), NDC 80425-0501-07, lot and expiration date (1/31/2027). It references comparison to ULTRAM and shows a barcode and pharmacy information.*

FDA Label Image

Tramadol HCl 50mg #240 (Tramadol HCl 50mg 80425 0501 08)

Tramadol Hydrochloride 50 mg coated tablet package label from Advanced Rx of Tennessee, LLC, Nashville, TN. The label includes the proprietary name, dosage strength, Rx-only status, and schedule classification (C-IV). It shows a barcode, NDC 80425-0501-08, and lot and expiration date fields. Instructions for storage at 20°-25°C (68°-77°F) and federal transfer cautions are also visible.*

FDA Label Image

1 (Tramadol Hydrochloride Tablets Usp 50 mg 1)

Chemical structure of tramadol hydrochloride shown as a skeletal formula with labeled functional groups, including methoxy (OCH3), hydroxyl (HO), and dimethylamino (N(CH3)2) groups along with the hydrochloride component (HCl).*

FDA Label Image

1 (Tramadol Hydrochloride Tablets Usp 50 mg 2)

A pharmacokinetic concentration-time graph depicting Tramadol and its metabolite M1 in plasma following single and multiple dosing. The y-axis shows concentration in ng/mL on a logarithmic scale, and the x-axis shows time in hours up to 48 h. Different line styles represent Tramadol multiple dose, Tramadol single dose, M1 multiple dose, and M1 single dose profiles.*

FDA Label Image

1 (Tramadol Hydrochloride Tablets Usp 50 mg 3)

A line chart titled 'Protocol CAPSS-047 Time to Discontinuation Due to Nausea/Vomiting' showing percent discontinuing on the y-axis against days in double-blind on the x-axis. Two stepwise lines compare discontinuation rates for 10 days versus 16 days to 200 mg/day dosing regimens, with the 10-day line showing higher discontinuation percentages over time.*

* 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.