Roflumilast Tablet
Product Images NDC 64380-786

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 Roflumilast (NDC 64380-786). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Strides Pharma Science Limited, 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

Structure (B6bf4503 9507 4aea Bcfe 362e2945c804 01)

Structure (B6bf4503 9507 4aea Bcfe 362e2945c804 01)
Chemical structure of roflumilast, illustrating its molecular connectivity including aromatic rings, fluorine substituents, oxygen, nitrogen, chlorine atoms, and functional groups consistent with its pharmaceutical composition.*
FDA Label Image

Figure 1 (B6bf4503 9507 4aea Bcfe 362e2945c804 02)

Figure 1 (B6bf4503 9507 4aea Bcfe 362e2945c804 02)
A forest plot chart showing the fold change in Cmax and AUC of roflumilast and its N-oxide relative to reference when coadministered with various drugs. The chart lists drugs on the vertical axis, with fold changes on the horizontal axis from 0 to 4, along with recommendations such as 'Use With Caution', 'No Dose Adjustment', and 'Not Recommended'.*
FDA Label Image

Container Label (B6bf4503 9507 4aea Bcfe 362e2945c804 03)

Container Label (B6bf4503 9507 4aea Bcfe 362e2945c804 03)
Roflumilast Tablets 500 mcg oral tablets packaging label by Strides Pharma Science Limited. The label includes dosage information, a barcode, NDC 64380-786-05, lot and expiration date fields, and a note indicating 90 tablets per package. It specifies prescription-only use and storage recommendations.*

* 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.