Hydrocodone Bitartrate And Ibuprofen
Product Images NDC 33261-378

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Hydrocodone Bitartrate And Ibuprofen (NDC 33261-378). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aidarex Pharmaceuticals Llc, 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 Ibu 7 5 200mg 1

Chemical structure depicting the active ingredient hydrocodone bitartrate, showing the molecular arrangement including aromatic rings, functional groups like methoxy and ketone, and the bitartrate component with its carboxyl and hydroxyl groups along with associated water molecules.*

FDA Label Image

Hydro Ibu 7 5 200mg 2

Chemical structure diagram of the active ingredient ibuprofen, showing its molecular arrangement including a carboxyl group and aromatic ring with attached methyl groups.*

FDA Label Image

Hydro Ibu 7 5 200mg 3

HYDROCODONE BITARTRATE AND IBUPROFEN bottle label showing a white plastic container with a white cap. The label displays the product name in capital letters along with dosage information, manufacturer Aidarex Pharmaceuticals LLC, and the product NDC number 33261-378. Specific dosage form, strength, and quantity details are not fully clear in the image provided.*

FDA Label Image

Hydro Ibu 7 5 200mg 4

Packaging label for HYDROCODONE BITARTRATE AND IBUPROFEN, 7.5/200 mg tablets by Aidarex Pharmaceuticals LLC. The package contains 60 film-coated tablets. The label displays the active ingredients with strengths and includes directions for use, NDC 33261-0378-60, and packaging information from Aidarex Pharmaceuticals LLC in Corona, CA.*

* 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.