Morphine Sulfate Tablet
Product Images NDC 0406-5118

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 Morphine Sulfate (NDC 0406-5118). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Specgx 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

Chemical Structure (Morphine Sulfate Ir 1)

Chemical Structure (Morphine Sulfate Ir 1)
Chemical structure of Morphine Sulfate showing the molecular arrangement including characteristic rings, hydroxyl groups, and nitrogen methyl group, along with sulfate and water molecules indicated.*
FDA Label Image

Principal Display Panel (15 mg Bottle)

Principal Display Panel (15 mg Bottle)
Morphine Sulfate 15 mg tablets label for oral use, containing 100 tablets per bottle. The label includes the NDC number 0406-5118-01, manufacturer SpecGx LLC, and dosing information that each tablet contains 15 mg of Morphine Sulfate USP. The label specifies prescription use (Rx only) and includes storage instructions and a note for pharmacists to dispense the Medication Guide separately. The tablet imprint shows the number '15', and the label also references manufacturer location in Webster Groves, MO.*
FDA Label Image

Principal Display Panel (30 mg Bottle)

Principal Display Panel (30 mg Bottle)
Morphine Sulfate Tablets 30 mg oral tablets in a blister pack. The label includes the NDC number 0406-5119-01 and indicates prescription use only (Rx only). It features dosage instructions, storage conditions, and a barcode, with the manufacturer listed as SpecGx LLC, Webster Groves, MO. The label also contains a partial image of a tablet.*

* 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.