Hydrocodone Bitartrate And Acetaminophen
Product Images NDC 67296-0299

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hydrocodone Bitartrate And Acetaminophen (NDC 67296-0299). 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

67296-0299 (Doc20161118143322 001)

Multiple Hydrocodone Bitartrate and Acetaminophen 5 mg/325 mg tablet labels from RedPharm Drug, Inc. are shown. Labels vary by tablet count including 4, 6, 10, 15, 20, 30, 50, and 60 tablets. Each label displays the drug name, strength, package size, Rx only designation, barcodes, storage instructions, lot number, expiration date, and manufacturing/distribution details.*

FDA Label Image

Hydro/apap (Doc20170810135612 001)

Multiple packaging labels for Hydrocodone Bitartrate and Acetaminophen Tablets USP 5mg/325mg by RedPharm Drug, Inc. Various tablet counts are shown including 4, 6, 10, 12, 15, 20, 30, 50, and 60 tablets. The labels include information such as NDC numbers, Rx only designation, storage instructions, manufacturer details (Amneal Pharmaceuticals of NY, Hauppauge, NY), and barcode images.*

FDA Label Image

Hydro/apap (Doc20171023142722 001)

Labels for Hydrocodone Bitartrate and Acetaminophen Tablets, USP 5mg/325mg by RedPharm Drug, Inc. The image shows multiple package sizes including 4, 6, 10, 12, 15, 20, 30, 40, 50, and 60 tablets. Each label includes NDC codes, barcodes, storage instructions, and manufacturer information from Amneal Pharmaceuticals of NY distributed by Redpharm Drug in Eden Prairie, MN.*

* 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.