Acetaminophen And Codeine Phosphate Tablet
Product Images NDC 80425-0530

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Acetaminophen And Codeine Phosphate (NDC 80425-0530). 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

Acetaminophen And Codeine 300/30mg #30 (Acetamino And Codeine 8025 0529 01)

Packaging label for Acetaminophen and Codeine Phosphate 300 mg/30 mg tablets. The label includes storage instructions, lot number, expiration date, and a note to compare to Tylenol with Codeine #3. It is labeled by Advanced Rx of Tennessee, LLC and indicates the product is a Schedule III controlled substance (C-III) for Rx only.*

FDA Label Image

Acetaminophen And Codeine 300/30mg #60 (Acetamino And Codeine 8025 0529 02)

Acetaminophen and Codeine Phosphate 300mg-30mg tablet label from Advanced Rx of Tennessee, LLC. The label includes dosing comparisons to Tylenol with Codeine #3, NDC numbers, expiration date of 08/31/2026, and a controlled substance designation (C-III). The packaging also includes storage instructions and manufacturer details.*

FDA Label Image

Acetaminophen And Codeine 300/30mg #90 (Acetamino And Codeine 8025 0529 03)

Packaging label for Acetaminophen and Codeine Phosphate 300 mg-30 mg tablets, distributed by Advanced Rx of Tennessee, LLC. The label includes storage instructions (20°-25°C), comparison information to Tylenol with Codeine #3, NDC codes (80425-0529-03 and 64850-0642-01), and notes the product is Schedule C-III and prescription only. Lot number and expiration date are partially redacted.*

FDA Label Image

Acetamino And Codeine 300/60mg #30 (Acetamino And Codeine 8025 0530 01)

Label for Acetaminophen and Codeine Phosphate 300 mg / 60 mg oral tablets. The label includes dosage form, strengths, and distributor information for Advanced Rx of Tennessee, LLC, Nashville, TN. Also displays NDC numbers, lot number, expiration date, and registration status as a Schedule III controlled substance (C-III). The label references comparison to Tylenol with Codeine #4 tablets.*

FDA Label Image

Acetamino And Codeine 300/60mg #60 (Acetamino And Codeine 8025 0530 02)

Label for Acetaminophen and Codeine Phosphate 300 mg / 60 mg oral tablets from Advanced Rx of Tennessee, LLC. Includes NDC numbers 80425-0530-02 and 64850-0643-01, lot number placeholder, and expiration date 12/31/2026. The label compares the product to Tylenol with Codeine #4 and includes storage instructions, barcode, and prescription-only designation (C-III).*

FDA Label Image

Acetamino And Codeine 300/60mg #90 (Acetamino And Codeine 8025 0530 03)

Label for Acetaminophen and Codeine Phosphate 300 mg/60 mg oral tablets by Advanced Rx of Tennessee, LLC. The label shows the product name, strength, NDC numbers, a storage temperature range (20°-25°C), a caution about transfer restrictions, and controlled substance classification C-III with Rx only. It also includes a barcode and manufacturing or lot information.*

FDA Label Image

Acetaminophen Molecular Structure (Acetaminophen Structure)

Chemical structure diagram of Acetaminophen and Codeine Phosphate, showing the molecular arrangement of the compound's atoms and bonds in a structural formula format.*

FDA Label Image

Codeine Phosphate Molecular Structure (Codeine Phosphate Structure)

Chemical structure of Acetaminophen and Codeine Phosphate, showing the molecular arrangement including a methoxy group, hydroxyl groups, and phosphate hydrate components as depicted in the image.*

* 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.