Hydrocodone Bitartrate And Acetaminophen
Product Images NDC 67296-1571

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Hydrocodone Bitartrate And Acetaminophen (NDC 67296-1571). 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

Hydroapap Label (Sdistributi18110615150 0001)

Two rectangular labels showing Hydrocodone Bitartrate and Acetaminophen 10/325MG tablets. Both indicate Rx Only status with lot numbers, expiration dates (05/20 and 02/20), and tablet counts (12 and 10). Labels include storage instructions, manufacturer Tris Pharma Inc. in Monmouth Junction, NJ, and distributor RedPharm Drug, Eden Prairie, MN. Barcodes and controlled substance schedule II markings appear on the right side.*

FDA Label Image

Hydro/apap 10/325 (Doc20180323150937 001)

Label for Hydrocodone Bitartrate and Acetaminophen 10/325 mg tablets, containing 20 tablets. The label shows the product is Rx Only, with an expiration date of April 2019. Manufacturer listed as Tris Pharma Inc., Monmouth Junction, NJ, and distributed by RedPharm Drug, Inc., Eden Prairie, MN. The label includes storage instructions and a barcode.*

* 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.