Inderal Xl Capsule, Extended Release
Product Images NDC 62559-601

4 FDA label images from Ani Pharmaceuticals, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Inderal Xl (NDC 62559-601). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ani Pharmaceuticals, 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

Ani (Ani)

FDA Label Image

Label-120mg (Label 120mg)

Label-120mg (Label 120mg)
This image shows a drug information label for Inderal XL (propranolol hydrochloride) Extended Release Capsules 120 mg. It includes usage instructions, storage conditions, distributor details (ANI Pharmaceuticals, Inc.), and manufacturer info (Adare Pharmaceuticals, Inc.). The label also displays an NDC number (62559-601-30), barcode, and specifies the package contains 30 capsules for prescription use only.*
FDA Label Image

Label-80mg (Label 80mg)

Label-80mg (Label 80mg)
Label for Inderal XL 80 mg extended release capsules containing propranolol hydrochloride. The label shows the product name, strength, dosage form, and quantity of 30 capsules. It includes the National Drug Code (NDC) 62559-600-30, and distributor ANI Pharmaceuticals, Inc. Storage instructions and dosing guidance are also present.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of propranolol hydrochloride. The diagram shows the molecular framework including naphthalene rings, an ether linkage, and amine group bonded to a substituted propane chain with hydrochloride indicated.*

* 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.