Hydrocodone Bitartrate And Acetaminophen Tablet
Product Images NDC 70010-673

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Hydrocodone Bitartrate And Acetaminophen (NDC 70010-673). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Granules 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

Hydroapap-structure-1 (Hydroapap Structure 1)

Chemical structure diagram of Hydrocodone Bitartrate and Acetaminophen, showing molecular components and including water of hydration (2 1/2 H2O) with molecular weight 494.490.*

FDA Label Image

Hydroapap-structure-2 (Hydroapap Structure 2)

Chemical structure diagram of acetaminophen, showing its molecular formula C8H9NO2 and molecular weight 151.16.*

FDA Label Image

Hydro-apap-5mg-325mg-100s (Hydro Apap 5mg 325mg 100s)

Label text for Hydrocodone Bitartrate and Acetaminophen Tablets USP, 5 mg/325 mg strength, details the active ingredient amounts per tablet and usual adult dosage instructions. It includes storage conditions, dispensing guidance, a mention of the accompanying Medication Guide, manufacturer details (Granules Pharmaceuticals Inc.), and a barcode.*

FDA Label Image

Hydro-apap-7-5mg-325mg-100s (Hydro Apap 7 5mg 325mg 100s)

Label for Hydrocodone Bitartrate and Acetaminophen Tablets, USP 7.5 mg/325 mg, oral tablet form. The label states the drug is for prescription use only, packaged as 100 tablets by Granules Pharmaceuticals Inc., Chantilly, VA. It includes dosage information, storage instructions, a barcode, and a note to dispense the accompanying medication guide to patients.*

FDA Label Image

Hydro-apap-10mg-325mg-100s (Hydro Apap 10mg 325mg 100s)

Label for Hydrocodone Bitartrate and Acetaminophen Tablets, USP with strength 10 mg/325 mg. The oral tablet product is prescription only, supplied in a package of 100 tablets, and labeled by Granules Pharmaceuticals Inc. Additional instructions include storage temperature and dosage guidance. The label features a barcode and a NDC number 70010-674-01.*

* 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.