Darunavir Tablet
Product Images NDC 60687-808

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Darunavir (NDC 60687-808). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

600 mg Darunavir Tablet Blister (600 mg Darunavir Tablet Blister)

600 mg Darunavir Tablet Blister (600 mg Darunavir Tablet Blister)
Sheet of multiple Darunavir 600 mg tablet labels from American Health Packaging. Each label shows the product name, strength, dosage form, barcodes, lot number, expiration date fields, and manufacturer information. Labels are arranged in two columns with identical content.*
FDA Label Image

600 mg Darunavir Tablets Carton (600 mg Darunavir Tablets Carton)

600 mg Darunavir Tablets Carton (600 mg Darunavir Tablets Carton)
Label for Darunavir 600 mg tablets by American Health Packaging. The label indicates a package of 30 tablets (3 x 10) for oral use and Rx only. It includes an alert about drug interactions, storage instructions, and a QR code for prescribing information, along with NDC and distributor details.*
FDA Label Image

800 mg Darunavir Tablet Blister (800 mg Darunavir Tablet Blister)

800 mg Darunavir Tablet Blister (800 mg Darunavir Tablet Blister)
Sheet of multiple labels for Darunavir 800 mg oral tablets from American Health Packaging. Each label includes the product name, dosage strength (800 mg), dosage form (tablet), a barcode, lot number, expiry date, and the labeler information with location Columbus, Ohio.*
FDA Label Image

800 mg Darunavir Tablets Carton (800 mg Darunavir Tablets Carton)

800 mg Darunavir Tablets Carton (800 mg Darunavir Tablets Carton)
Darunavir 800 mg tablets label showing the product name, dosage strength, form, and quantity of 30 tablets (3 x 10). The label includes a barcode, storage instructions, caution regarding medicine interactions, and distributor information for American Health Packaging. It is marked Rx Only and contains a QR code for prescribing information.*
FDA Label Image

Ahp80821

Ahp80821
Darunavir 600 mg or 800 mg oral tablet, white, oblong with imprint 'C2L8' on one side and plain on the other. Manufactured by American Health Packaging.*
FDA Label Image

Ahp81921

Ahp81921
Darunavir 600 mg or 800 mg oral tablet, white, oblong with a score line on one side and the imprint 'C247' on the same side. The other side is plain. Manufactured by American Health Packaging.*
FDA Label Image

Structural Formula (Structure)

Structural Formula (Structure)
Chemical structure of Darunavir, showing its molecular arrangement including sulfonamide and amide functional groups, along with associated side chains. The figure also indicates the presence of 2.5 water molecules (2.5 H2O) in its hydrated form.*
FDA Label Image

Figure 1: Pharmacokinetic Results (within-subject Comparison) Of Total And Unbound Darunavir After Administration Of Darunavir/ritonavir At 600/100 mg Twice Daily Or 800/100 mg Once Daily As Part Of A (Fig 02)

Figure 1: Pharmacokinetic Results (within-subject Comparison) Of Total And Unbound Darunavir After Administration Of Darunavir/ritonavir At 600/100 mg Twice Daily Or 800/100 mg Once Daily As Part Of A (Fig 02)
Two side-by-side charts compare pharmacokinetic parameters of Darunavir/ritonavir during the second and third trimesters. The left chart shows twice daily dosing and the right chart shows once daily dosing. Parameters include total and unbound AUC and Cmin with GMR values and 90% confidence intervals indicated by markers and error bars.*

* 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.