Simvastatin Tablet, Film Coated
Product Images NDC 51655-387

4 FDA label images from Northwind Health Company, Llc · 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 51655-387). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, 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

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

Image (Bf184423 4257 4ef1 9b71 3a829fd8e30d 01)
Chemical structure diagram of simvastatin, showing its molecular configuration with functional groups and ring systems typical of this active ingredient.*
FDA Label Image

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

Image (7c509112 Dd21 4383 9c46 59cd44d91d73 130 1)
SIMVASTATIN 40 mg film-coated tablets are shown in a blister pack with 10 tablets arranged in two rows of five. The blister pack has a white background with some black printed text and a distinctive pattern of black clover-like symbols down the center. The labeler is Northwind Health Company, LLC.*
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 carton by Northwind Health Company, LLC. The white and red carton features the SIMVASTATIN brand name prominently along with the dosage strength of 40 mg. The package contains tablets for oral use, indicated by the film-coated tablets partially visible beside the carton.*
FDA Label Image

Label (51655 387 26 Rev A 03 23 Nhc)

Label (51655 387 26   Rev A 03 23 Nhc)
This is a label for Simvastatin Tablets USP 40 mg by Northwind Health Company, LLC. The label indicates the product contains 90 film-coated tablets for oral use, with storage instructions and a note to see the package insert for dosage. The label includes the NDC 51655-387-26 and warnings about keeping out of reach of children and storing in the original container.*

* 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.