Hydrocodone Bitartrate And Acetaminophen Tablet
Product Images NDC 70010-673

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 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

70010 672 01 Jpg

70010 672 01 Jpg
Label for Hydrocodone Bitartrate and Acetaminophen Tablets, USP 5 mg/325 mg, oral tablets. This prescription drug label from Granules Pharmaceuticals Inc. includes dosage strength, administration instructions, storage conditions, barcode, and package size of 100 tablets. The label emphasizes dispensing the accompanying Medication Guide and keeping medication out of children's reach.*
FDA Label Image

70010 673 01 Jpg

70010 673 01 Jpg
Label for Hydrocodone Bitartrate and Acetaminophen Tablets, USP 7.5 mg/325 mg, oral tablet by Granules Pharmaceuticals Inc. The label includes NDC 70010-673-01, dosage strength, quantity of 100 tablets, storage instructions, and a barcode. It notes the prescription-only status and advises dispensing the accompanying medication guide.*
FDA Label Image

70010 674 01 Jpg

70010 674 01 Jpg
Label for Hydrocodone Bitartrate and Acetaminophen Tablets USP, 10 mg/325 mg strength. The label indicates 100 tablets in the package, manufactured by Granules Pharmaceuticals Inc. It includes dosage information, storage instructions, and a barcode.*
FDA Label Image

Hydro Apap 10mg Label Jpg

Hydro Apap 10mg Label Jpg
Label for Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/325 mg. The label states the product is an oral tablet containing 10 mg of Hydrocodone Bitartrate and 325 mg of Acetaminophen. It includes dispensing instructions, dosage guidelines for adults, storage recommendations, and a reminder to dispense the medication guide. The label indicates Rx only and a package size of 500 tablets. Manufactured by Granules Pharmaceuticals Inc., Chantilly, VA.*
FDA Label Image

Hydro Apap 5mg Label Jpg

Hydro Apap 5mg Label Jpg
Label for Hydrocodone Bitartrate and Acetaminophen tablets, USP, containing 5 mg hydrocodone bitartrate and 325 mg acetaminophen per tablet. The label indicates it is for prescription use only, with a package quantity of 500 tablets. It is manufactured by Granules Pharmaceuticals Inc. and includes dosing and storage instructions, along with a barcode and regulatory information.*
FDA Label Image

Hydro Apap 7 5mg Label Jpg

Hydro Apap 7 5mg Label Jpg
Label for Hydrocodone Bitartrate and Acetaminophen Tablets, USP 7.5 mg/325 mg, oral tablets by Granules Pharmaceuticals Inc. The label includes NDC 70010-673-05, directions for use, storage instructions, and a quantity of 500 tablets. It highlights the active ingredients per tablet and states the product is prescription only.*
FDA Label Image

Hydroapap-structure-1-jpg (Hydroapap Structure 1 Jpg)

Hydroapap-structure-1-jpg (Hydroapap Structure 1 Jpg)
Chemical structure of hydrocodone bitartrate dihydrate, showing molecular formula C18H21NO3·C4H6O6·2 1/2 H2O and molecular weight 494.90.*
FDA Label Image

Hydroapap-structure-2-jpg (Hydroapap Structure 2 Jpg)

Hydroapap-structure-2-jpg (Hydroapap Structure 2 Jpg)
Chemical structure diagram of acetaminophen, showing its molecular formula (C8H9NO2) and molecular weight (151.16). The structure includes an acetyl group connected to a phenol ring with a hydroxyl group.*

* 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.