Hydrocodone Bitartrate And Acetaminophen
Product Images NDC 68387-230

3 FDA label images from Keltman Pharmaceuticals Inc. · Packaging, Regulatory Labels, and Product Appearance

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 68387-230). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Keltman 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

Acetaminophen-structure (Acetaminophen Str)

Acetaminophen-structure (Acetaminophen Str)
Chemical structure of acetaminophen, showing a benzene ring with hydroxyl and amide functional groups attached.*
FDA Label Image

Hydrocodone-structure (Hydrocodone Structure)

Hydrocodone-structure (Hydrocodone Structure)
Chemical structure diagram showing three distinct components: hydrocodone molecule on the left, tartaric acid molecule in the center, and water molecules represented as 5/2H2O on the right, illustrating the chemical composition of hydrocodone bitartrate hydrate.*
FDA Label Image

Hydrocodone Bitartrate And Acetaminophen (Label)

Hydrocodone Bitartrate And Acetaminophen (Label)
HYDROCODONE BITARTRATE AND ACETAMINOPHEN 7.5mg/500mg tablet label by Keltman Pharmaceuticals Inc. The label shows product identifiers including NDC 68387-230-40, lot number 83945A1, expiration date 2/2011, and Rx number 98495. The package contains 40 tablets, each with 7.5 mg hydrocodone bitartrate and 500 mg acetaminophen. Storage instructions specify controlled room temperature 68-77°F. It includes caution about federal law and distribution details from Watson Laboratories and Keltman Pharmaceuticals.*

* 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.