Hydrocodone Bitartrate And Acetaminophen
Product Images NDC 67296-1377

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 67296-1377). 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

Hydro/apap 7.5/325 (Doc20170524151518 001)

This is a description of a prescription drug labeled as a controlled substance. The drug contains a combination of hydrocodone bitartrate and acetaminophen with a strength of 7.5/325mg. It comes in a package of 6 tablets, with a lot number of F24416 and an expiration date of 06/18. The usual adult dosage is not specified on the label, and it must be obtained from the package insert. The drug should be stored at a controlled room temperature of 20-25 C (68-77 F). The manufacturer is Amneal Pharmaceuticals of NY with a distribution by Redpharm Drug in Eden Prairie, MN.*

FDA Label Image

Hydro/apap (Doc20171023152426 001)

This is a prescription drug containing Hydrocodone Bitartrate and Acetaminophen in the strength of 7.5mg and 325mg respectively. The package contains 30 tablets in a Lot number K28816 1 Exp: 10/18. The usual dosage for adults is provided in the package insert. The drug should be stored in a controlled room temperature between 20-25 C (68-77 F). The drug is manufactured by Amneal Pharmaceuticals of NY located in Hauppauge NY 11788 and distributed by Redpharm Drug, Eden Prairie, MN 55344 with the national drug code (NDC) 67296-1377-3 and SIN number 209888.*

* 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.