Nisoldipine
Product Images NDC 0677-1981

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Nisoldipine (NDC 0677-1981). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by United Research Laboratories, Inc., 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

Chemical Structure (Nisoldipine 01)

Chemical structure diagram of Nisoldipine, showing its molecular framework and functional groups including nitro, ester, and methyl substituents.*

FDA Label Image

Principal Display Panel (8.5 mg label)

Label for Nisoldipine Extended Release Tablets 8.5 mg by United Research Laboratories, Inc. The label indicates the product contains 100 tablets and is Rx only. The label includes storage instructions, manufacturing and packaging details, lot number, and expiration date areas.*

FDA Label Image

Principal Display Panel (8.5 mg carton)

Packaging label for Nisoldipine Extended Release Tablets 8.5 mg by United Research Laboratories, Inc. The label includes the product name, strength, dosage form, quantity of 100 tablets, and instructions to see the package insert for full prescribing information. Manufacturer information and barcode are also displayed.*

FDA Label Image

Principal Display Panel 17 mg Label (Nisoldipine 04)

Nisoldipine Extended Release Tablets 17 mg label by United Research Laboratories, Inc. The label includes the product name, strength, dosage form, count of 100 tablets, manufacturer address in Philadelphia, PA, and storage instructions. The label also features a barcode and fields for lot number and expiration date.*

FDA Label Image

Principal Display Panel 17 mg Carton (Nisoldipine 05)

Nisoldipine Extended Release Tablets 17 mg packaging label by United Research Laboratories, Inc. The label displays the product name, strength, dosage form, quantity of 100 tablets, and storage instructions. It includes barcodes and manufacturing information, including that it is made in France and for United Research Laboratories, Inc. The label instructs to see the package insert for full prescribing information.*

FDA Label Image

Principal Display Panel (25.5 mg label)

Nisoldipine Extended Release Tablets 25.5 mg label from United Research Laboratories, Inc. The label indicates a package containing 100 tablets for prescription use only. It includes storage instructions, manufacturing information, and regulatory codes. The label is predominantly blue, white, and red.*

FDA Label Image

Principal Display Panel (25.5 mg carton)

Nisoldipine Extended Release Tablets 25.5 mg packaging label from United Research Laboratories, Inc. The label shows dosage strength and instructions to see the package insert for full prescribing information. It includes storage instructions and manufacturer details. The package size is indicated as 100 tablets for prescription use only.*

FDA Label Image

Principal Display Panel 34 mg Label (Nisoldipine 08)

Nisoldipine Extended Release Tablets 34 mg label from United Research Laboratories, Inc., Philadelphia, PA. The label includes the NDC number 06771-1981-01 and indicates a bottle containing 100 tablets. It features storage instructions, National Drug Code information, and space for lot number and expiration date.*

FDA Label Image

Principal Display Panel (34 mg carton)

Packaging label for Nisoldipine Extended Release Tablets 34 mg by United Research Laboratories, Inc. The label indicates the product is for prescription use only and comes in a bottle containing 100 tablets. Storage instructions and manufacturer information are visible on the label.*

* 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.