Lovastatin Tablet
Product Images NDC 51655-558

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 Lovastatin (NDC 51655-558). 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.

Product Images & Figures Index

FDA Label Image

Label (51655 558 26 Master Bottle Label Approval Rev A 01 21)

Label (51655 558 26 Master Bottle Label Approval Rev A 01 21)
Label for Lovastatin Tablets, USP 20 mg oral tablets. The package contains 90 tablets and is labeled Rx Only. Manufacturer is Northwind Health Company, LLC. Storage instructions include storing at 25°C with permitted excursions and protecting from light. NDC is 51655-558-26.*
FDA Label Image

Lovastatin (65abb8c3 847f 4fb3 B8de 21888c01210b 01)

Lovastatin (65abb8c3 847f 4fb3 B8de 21888c01210b 01)
Chemical structure diagram of lovastatin, the active ingredient in Lovastatin 20 mg oral tablets by Northwind Health Company, LLC. The diagram shows the molecular arrangement and bonding of atoms in the lovastatin molecule.*
FDA Label Image

Figure 1 (65abb8c3 847f 4fb3 B8de 21888c01210b 02)

Figure 1 (65abb8c3 847f 4fb3 B8de 21888c01210b 02)
A line graph titled 'Figure 1 Acute Major Coronary Events (Primary Endpoint)' comparing the proportion of participants without events over 6 years of follow-up between Lovastatin and Placebo groups. The graph shows higher event-free proportions for the Lovastatin group, with a marked 37% risk reduction indicated near the end of the follow-up period.*

* 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.