Propranolol Hydrochloride
Product Images NDC 60760-576

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 Propranolol Hydrochloride (NDC 60760-576). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by St. Mary's Medical Park Pharmacy, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

576-30 (Propranolol 576 30)

576-30 (Propranolol 576 30)
Label for Propranolol Hydrochloride Extended-Release Capsules USP 80 mg, quantity 30. Manufactured by Yichang Humanwell Oral Solid Dosage Plant in China; packaged by St. Mary's Medical Park Pharmacy in Oro Valley, AZ. Includes NDC 60760-576-30 and storage instructions for controlled room temperature (15-30°C or 59-86°F).*
FDA Label Image

Chemical-structure (Propranolol Hydrochloride Extended Release Capsule 1)

Chemical-structure (Propranolol Hydrochloride Extended Release Capsule 1)
Chemical structure of Propranolol Hydrochloride, showing the arrangement of its molecular components including naphthalene, hydroxyl, ether linkages, and amine groups with the hydrochloride salt.*
FDA Label Image

Ink (Propranolol Hydrochloride Extended Release Capsule 3)

Ink (Propranolol Hydrochloride Extended Release Capsule 3)
Propranolol Hydrochloride 40 mg tablets blister pack from ST. MARY'S MEDICAL PARK PHARMACY. The strip contains 10 round, yellow tablets arranged in two rows of five with printed identification on each tablet. The pack is labeled with the product name, strength, and includes dosage form information.*

* 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.