Simvastatin Tablet, Film Coated
Product Images NDC 50090-4736

4 FDA label images from A-s Medication Solutions · 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 Simvastatin (NDC 50090-4736). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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

Image (Bf184423 4257 4ef1 9b71 3a829fd8e30d 01)

Image (Bf184423 4257 4ef1 9b71 3a829fd8e30d 01)
Chemical structure of simvastatin, shown as a molecular diagram with rings, bonds, and functional groups including hydroxyl and ketone groups, consistent with the known structure of the active ingredient simvastatin.*
FDA Label Image

Image (7c509112 Dd21 4383 9c46 59cd44d91d73 130 1)

Image (7c509112 Dd21 4383 9c46 59cd44d91d73 130 1)
SIMVASTATIN 40 mg film-coated tablet by A-S Medication Solutions, displayed as a round, white tablet with one side showing the imprint '4736' and the other side plain, illustrating the oral dosage form for this human prescription drug.*
FDA Label Image

Image (7c509112 Dd21 4383 9c46 59cd44d91d73 182 1)

Image (7c509112 Dd21 4383 9c46 59cd44d91d73 182 1)
SIMVASTATIN 40 mg film-coated tablets in a clear plastic blister pack with 10 oval-shaped tablets arranged in two rows of five each, produced by A-S Medication Solutions. The tablets are pale, light-colored, and unprinted, contained within a transparent cover sealed to a white backing card.*
FDA Label Image

Label Image (Lbl500904736)

Label Image (Lbl500904736)
SIMVASTATIN 40 mg film-coated tablets packaging label by A-S Medication Solutions. The label indicates 100 tablets per container, storage instructions between 68-77 degrees Fahrenheit, and a caution to see the dosage page insert. The product is an oral human prescription drug with NDC 50090-4736.*

* 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.