Hydrocodone Bitartrate And Acetaminophen
Product Images NDC 67296-1334

1 FDA label image from Redpharm Drug, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Hydrocodone Bitartrate And Acetaminophen (NDC 67296-1334). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Hydrocodone/apap 7.5/325 (Doc20170522161248 001)

Hydrocodone/apap 7.5/325 (Doc20170522161248 001)
Label for Hydrocodone Bitartrate and Acetaminophen tablets, strength 7.5 mg/325 mg, containing 30 tablets. The label includes NDC 67296-1334-3, marked Rx Only, with lot number 900201 1 and expiration date 04/17. Manufactured by Halo Pharmaceutical Inc., Whippany, NJ, and distributed by RedPharm Drug, Eden Prairie, MN. Storage instructions specify controlled room temperature 20-25°C (68-77°F). The label also features a barcode and a class II controlled substance mark.*

* 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.