Hydrocodone Bitartrate And Acetaminophen Tablet
Product Images NDC 72865-201

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Hydrocodone Bitartrate And Acetaminophen (NDC 72865-201). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Xlcare Pharmaceuticals, Inc., 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

10 mg (10 mg 100s)

Label for Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/325 mg by XLCare Pharmaceuticals, Inc. The label includes the NDC number 72865-204-01 and states the package contains 100 tablets. It features dosing information, storage instructions, manufacturer details, and a directive to dispense the medication guide to patients.*

FDA Label Image

10 mg (10 mg 500s)

Label for Hydrocodone Bitartrate and Acetaminophen Tablets USP, 10 mg/325 mg strength, oral tablets by XLCare Pharmaceuticals, Inc. The label indicates 500 tablets per bottle, prescription only, and specifies the package is not child-resistant. It includes storage instructions and advises dispensing the Medication Guide separately.*

FDA Label Image

2.5 mg (2.5 mg 100s)

Label for Hydrocodone Bitartrate and Acetaminophen Tablets, USP 2.5 mg/325 mg, oral tablets by XLcare Pharmaceuticals, Inc. The label indicates a count of 100 tablets and includes instructions for pharmacists to dispense the Medication Guide separately. Storage and usage directions, manufacturer details, and NDC 72865-201-01 are also visible.*

FDA Label Image

5 mg (5 mg 100s)

Label for Hydrocodone Bitartrate and Acetaminophen Tablets, USP 5 mg/325 mg by XLCare Pharmaceuticals, Inc. The label states 100 tablets, prescription only. It includes dosage strength, storage instructions, dispensing precautions, manufacturer information, and a barcode. The label design features a blue and yellow accent with drug name and strength prominently displayed.*

FDA Label Image

5 mg (5 mg 500s)

Packaging label for Hydrocodone Bitartrate and Acetaminophen tablets, USP 5 mg/325 mg, oral tablets by XLCare Pharmaceuticals Inc. The label shows NDC 72865-202-05, package size of 500 tablets, and indicates the package is not child-resistant. It includes storage instructions, dispensing information, and manufacturer details with addresses in Georgia and New York.*

FDA Label Image

7.5 mg (7.5 mg 100s)

Label for Hydrocodone Bitartrate and Acetaminophen Tablets, USP 7.5 mg/325 mg by XLCare Pharmaceuticals, Inc. The oral tablet package contains 100 tablets. The label includes storage instructions, dosage strength, manufacturer details, and a notice for pharmacists to dispense a medication guide with each prescription.*

FDA Label Image

7.5 mg (7.5 mg 500s)

Label for Hydrocodone Bitartrate and Acetaminophen Tablets, USP, 7.5 mg/325 mg strength by XLCare Pharmaceuticals, Inc. The oral tablets package contains 500 tablets and is marked Rx only. The label notes the package is not child-resistant and includes storage instructions and drug strengths. Manufacturer details and regulatory information are also provided.*

FDA Label Image

Hydrocodone Bitartrate- Structure (Struct1)

Chemical structure diagram showing the molecular formulas of hydrocodone bitartrate and acetaminophen, including water of hydration (2.5 H2O). The molecular weight is indicated as 494.490.*

FDA Label Image

Acetaminophen- Structure (Struct2)

Chemical structure of acetaminophen, showing its molecular arrangement with a phenol group and acetamide group, labeled with molecular formula C8H9NO2 and molecular weight 151.16.*

* 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.