Nebivolol Tablet
Product Images NDC 72603-873

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Nebivolol (NDC 72603-873). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rxllc, 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

505 (Nebivolol 10 mg 30s)

505 (Nebivolol 10 mg 30s)
Nebivolol Tablets 10 mg package label displaying the product name, strength, and quantity of 30 tablets. The label includes storage instructions, barcode, NDC number 72603-872-01, manufacturer information (NorthStar Rx LLC, Memphis, TN) and Macleods Pharmaceuticals Ltd., India), and safety warnings such as keeping out of reach of children and using child-resistant containers.*
FDA Label Image

505 (Nebivolol 10 mg 90s)

505 (Nebivolol 10 mg 90s)
Nebivolol Tablets 10 mg oral tablet label displaying the product name, strength, and quantity of 90 tablets. The label includes storage instructions, dosage guidance referencing the package insert, and child-resistant packaging requirements. It shows the manufacturer as Macleods Pharmaceuticals Ltd. in India and the labeler as NorthStar Rx LLC, Memphis, TN.*
FDA Label Image

505 (Nebivolol 2 5 mg 30s)

505 (Nebivolol 2 5 mg 30s)
Nebivolol Tablets 2.5 mg label for oral tablets, containing 30 tablets per package. The label includes storage instructions, dosage advisory, and manufacturer details. It is labeled as Rx only and manufactured by Macleods Pharmaceuticals Ltd. for NorthStar Rx LLC, Memphis, TN.*
FDA Label Image

505 (Nebivolol 20 mg 30s)

505 (Nebivolol 20 mg 30s)
Nebivolol Tablets 20 mg oral tablet label by NorthStar Rx LLC. The label includes storage instructions, usage directions referencing package insert, and the drug is supplied in a bottle of 30 tablets. Manufacturer is Macleods Pharmaceuticals Ltd., India. NDC 72603-873-01.*
FDA Label Image

505 (Nebivolol 20 mg 90s)

505 (Nebivolol 20 mg 90s)
Nebivolol Tablets 20 mg oral tablets packaging label from NorthStar Rx LLC. The label specifies a count of 90 tablets, includes dosage and storage information, and lists manufacturer details as Macleods Pharmaceuticals Ltd., India. The label features a barcode and an NDC number 72603-873-02.*
FDA Label Image

505 (Nebivolol 5 mg 30s)

505 (Nebivolol 5 mg 30s)
Nebivolol Tablets 5 mg oral tablets packaging label showing a 30-tablet bottle. The label includes the NDC 72603-871-01 and indicates the product is manufactured by Macleods Pharmaceuticals Ltd. for NorthStar Rx LLC. Storage instructions and barcodes are also visible. The label displays a blue and white color scheme with orange highlighting the 5 mg strength.*
FDA Label Image

505 (Nebivolol 5 mg 90s)

505 (Nebivolol 5 mg 90s)
Nebivolol Tablets 5 mg oral tablet packaging label from NorthStar Rx LLC. The label states each tablet contains 5 mg of nebivolol hydrochloride. The package contains 90 tablets and includes storage instructions and manufacturer information, listing Macleods Pharmaceuticals Ltd., India as the manufacturer.*
FDA Label Image

Str-1 (Nebivolol Str 1)

Str-1 (Nebivolol Str 1)
Chemical structure of d-nebivolol hydrochloride, showing molecular composition and arrangement of atoms in the compound known as Nebivolol.*
FDA Label Image

Str-2 (Nebivolol Str 2)

Str-2 (Nebivolol Str 2)
Chemical structure of Nebivolol hydrochloride, showing the molecular configuration and labeled with its molecular weight of 441.90 g/mol.*

* 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.