Oxycodone And Acetaminophen Tablet
Product Images NDC 10702-185

Product Visual Gallery

This gallery contains 15 technical images submitted to the FDA as part of the official labeling for Oxycodone And Acetaminophen (NDC 10702-185). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kvk-tech, 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

09d5e06a Figure 10

Label for Oxycodone and Acetaminophen Tablets, USP, 7.5 mg/325 mg, oral tablets provided by KVK-Tech, Inc. The label includes dosage strength, NDC number 10702-186-01, storage instructions, dispensing warnings, and regulatory requirements such as DEA order form and tamper-evident seal information. The package contains 100 tablets and notes that multiple strengths are available.*

FDA Label Image

09d5e06a Figure 11

Label for Oxycodone and Acetaminophen Tablets USP, strength 7.5 mg/325 mg, oral tablet form. The label includes NDC 10702-186-50, manufacturer KVK-Tech, Inc., and package size of 500 tablets. It contains directions on dispensing, storage, warnings, and DEA order form requirement, with a barcode on the right side.*

FDA Label Image

09d5e06a Figure 12

Label for Oxycodone and Acetaminophen Tablets, USP containing 7.5 mg oxycodone hydrochloride and 325 mg acetaminophen per tablet. The label states multiple strengths are available and cautions to dispense only if strength is stated. It includes dosing, storage, and safety instructions, and indicates the product is manufactured by KVK-Tech, Inc. This package contains 1000 tablets with NDC 10702-186-10.*

FDA Label Image

09d5e06a Figure 13

Label for Oxycodone and Acetaminophen Tablets, USP, containing 10 mg oxycodone hydrochloride and 325 mg acetaminophen per tablet. The label notes multiple strengths are available and cautions not to dispense unless the stated strength is specified. Packaged by KVK-Tech, Inc., Newtown, PA, containing 100 tablets. Instructions include dispensing a medication guide and storage at 20° to 25°C with child-resistant packaging. The label also states that a DEA order form is required and provides a barcode.*

FDA Label Image

09d5e06a Figure 14

Oxycodone and Acetaminophen Tablets USP 10 mg/325 mg oral tablets label. The label displays active ingredient strengths, dosage instructions, storage conditions, and safety warnings. It includes NDC 10702-187-50, quantity of 500 tablets, and the labeler KVK-Tech, Inc. The label cautions about multiple strengths and prescription-only status.*

FDA Label Image

09d5e06a Figure 15

Oxycodone and Acetaminophen Tablets, USP oral tablets with strength 10 mg oxycodone and 325 mg acetaminophen per tablet. The label indicates a package size of 1000 tablets, manufactured by KVK-Tech, Inc., Newtown, PA. The label includes storage information, dispensing warnings, and a barcode.*

FDA Label Image

Container Label (2.5 mg/325 mg)

Label for Oxycodone and Acetaminophen Tablets, USP, showing strength 2.5 mg/325 mg. The label includes dosage details, storage instructions, warnings, and regulatory information. It is marked Rx Only, contains 100 tablets, and is manufactured by KVK-Tech, Inc., Newtown, PA. The label also features a barcode and specifies the need for a DEA order form and child-resistant packaging.*

FDA Label Image

Container Label (7.5 mg/325 mg)

Oxycodone and Acetaminophen Tablets USP, 2.5 mg/325 mg oral tablets, packaged by KVK-Tech, Inc. The label includes dosage information, dispensing instructions, storage conditions, and a barcode. The container holds 500 tablets and indicates prescription-only status with tamper-evident foil seal instructions.*

FDA Label Image

Container Label (5 mg/325 mg)

Oxycodone and Acetaminophen Tablets USP label with 2.5 mg oxycodone and 325 mg acetaminophen per tablet. The label includes dosage and storage instructions, a warning to keep medications out of reach of children, and states that a DEA order form is required. It is manufactured by KVK-Tech, Inc., with a package size of 1000 tablets shown.*

FDA Label Image

Container Label (10 mg/325 mg)

Label for Oxycodone and Acetaminophen Tablets, USP showing strength 5 mg/325 mg in tablet form. The label includes a warning about multiple strengths, dispensing instructions, storage conditions, and required DEA order form. Labeler is KVK-Tech, Inc., Newtown, PA. The package size states 100 tablets.*

FDA Label Image

09d5e06a Figure 8

Oxycodone and Acetaminophen tablets USP 5 mg/325 mg oral tablets packaging label from KVK-Tech, Inc. The label states the active ingredients as oxycodone hydrochloride 5 mg and acetaminophen 325 mg per tablet, in a bottle containing 500 tablets. Important instructions include storing at controlled room temperature and keeping out of reach of children. The label notes a DEA order form is required and cautions about tamper-evident seals.*

FDA Label Image

09d5e06a Figure 9

Packaging label for Oxycodone and Acetaminophen Tablets, USP, with strength of 5 mg/325 mg. The label indicates 1000 tablets in the container, manufactured by KVK-Tech, Inc. It includes prescription warnings, storage instructions, and notes multiple strengths are available, emphasizing dispensing only when strength is stated.*

FDA Label Image

Chemical Structure Apap

Chemical structure of Acetaminophen with its molecular formula (C8H9NO2) and molecular weight (151.16) displayed alongside the structural diagram.*

FDA Label Image

Chemical Structure Oxy

Chemical structure of oxycodone hydrochloride showing its molecular formula C18H21NO4•HCl and molecular weight 351.82. The diagram depicts the arrangement of atoms and bonds in the oxycodone molecule.*

FDA Label Image

Company Logo

* 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.