Hydrocodone Bitartrate And Acetaminophen
Product Images NDC 45865-605

4 FDA label images from Medsource Pharmaceticals · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Hydrocodone Bitartrate And Acetaminophen (NDC 45865-605). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medsource Pharmaceticals, 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

Pdp75 (419 60)

Pdp75 (419 60)
Packaging label for Hydrocodone Bitartrate and Acetaminophen tablets, 7.5 mg/325 mg strength. The label indicates a count of 60 tablets in the package and that the product is generic for Norco. It shows the labeler as Medsource Pharmaceuticals with qualitative description and dosage instructions visible.*
FDA Label Image

Pdp (605 60)

Pdp (605 60)
Label for Hydrocodone Bitartrate and Acetaminophen tablets, each 5 mg/325 mg, generic for Norco CII. The package contains 60 tablets. The label includes warnings about habit-forming potential, dizziness, drowsiness, and alcohol avoidance. Manufactured by Medsource Pharmaceuticals.*
FDA Label Image

Apapstructure (Apapstructure)

Apapstructure (Apapstructure)
Chemical structure of the active ingredient Hydrocodone Bitartrate And Acetaminophen, showing molecular components and molecular weight of 151.16.*
FDA Label Image

Hydrostructure (Hydrostructure)

Hydrostructure (Hydrostructure)
Chemical structure diagram of Hydrocodone Bitartrate Dihydrate, showing molecular formula C18H21NO3 · C4H6O6 · 2.5H2O and molecular weight 494.5, from the Medsource Pharmaceuticals label.*

* 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.