Hydrocodone Bitartrate And Acetaminophen
Product Images NDC 45865-412

View Photos of 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 45865-412). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medsource Pharmaceuticals, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Image From Drug Label Content (Hydrocodone Bit Apap 7point5 650mg 1)

Image From Drug Label Content (Hydrocodone Bit Apap 7point5 650mg 1)
Chemical structure of Hydrocodone Bitartrate, depicting the molecular arrangement including rings and functional groups, accompanied by the bitartrate component and two molecules of water of hydration (2H2O).*
FDA Label Image

Image From Drug Label Content (Hydrocodone Bit Apap 7point5 650mg 2)

Image From Drug Label Content (Hydrocodone Bit Apap 7point5 650mg 2)
Chemical structure of hydrocodone bitartrate and acetaminophen, showing a benzene ring with hydroxyl (OH) and acetamido (NHCOCH3) functional groups attached.*
FDA Label Image

Bottle Of 30 (Hydrocodone Bit Apap 7point5 650mg 3)

Bottle Of 30 (Hydrocodone Bit Apap 7point5 650mg 3)
Hydrocodone Bitartrate and Acetaminophen tablets 7.5 mg / 650 mg, generic for Lortec Plus, in a unit dose package of 30 tablets. The label includes warnings about dizziness and drowsiness, advising not to drive or operate machinery. Instructions indicate to take one tablet every specified hours as needed for pain, with bilingual English and Spanish text. The product is labeled by Medsource Pharmaceuticals and includes the NDC 45865-0412-30.*

* 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.