Propranolol Hydrochloride Capsule, Extended Release
Product Images NDC 0527-4118

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Propranolol Hydrochloride (NDC 0527-4118). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lannett Company, 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

Structure (Propranolol Hydrochloride Extended Release Capsule 1)

Chemical structure of propranolol hydrochloride depicted with its characteristic aromatic rings and side chains including hydroxyl and amine groups, alongside the hydrochloride (HCl) component.*

FDA Label Image

Logo (Propranolol Hydrochloride Extended Release Capsule 2)

Propranolol Hydrochloride extended release capsules packaging from Lannett Company, Inc. The label shows the propranolol hydrochloride capsules with a strength of 120 mg. The capsules contain 60 count each, identified as an oral prescription drug.*

FDA Label Image

Logo (Propranolol Hydrochloride Extended Release Capsule 3)

Propranolol Hydrochloride extended-release capsules in a white and red blister pack with 15 capsules shown. The packaging indicates multiple strengths available, manufactured by Lannett Company, Inc. The capsules are designed for oral administration.*

FDA Label Image

Logo (Propranolol Hydrochloride Extended Release Capsule 4)

Propranolol Hydrochloride extended-release capsules in a blister pack, labeled with strength of 80 mg. The packaging is white with black and yellow markings, showing capsule count and dosage form. The manufacturer is Lannett Company, Inc.*

FDA Label Image

Logo (Propranolol Hydrochloride Extended Release Capsule 5)

Propranolol Hydrochloride 80 mg extended release oral capsules in a white blister pack with a grid of 14 capsules. Each capsule is white and gray with visible imprint. The packaging is intended for human prescription use by Lannett Company, Inc.*

FDA Label Image

60 mg (Propranolol Hydrochloride Extended Release Capsule 6)

Label for Propranolol Hydrochloride Extended-Release Capsules, USP, 60 mg. This human prescription drug is supplied as oral extended-release capsules by Lannett Company, Inc. The label includes dosage strength (60 mg), package size (100 capsules), storage instructions, and manufacturer details. It also states 'No Varnish' on the side.*

FDA Label Image

80 mg (Propranolol Hydrochloride Extended Release Capsule 7)

Label for Propranolol Hydrochloride Extended-Release Capsules, USP, 80 mg strength. The label includes dosage form as extended-release capsules and package count of 100 capsules. It shows that the product is distributed by Lannett Company, Inc. and manufactured by Yichang Humanwell Oral Solid Dosage Plant in China. The label also advises storage conditions and child safety warnings.*

FDA Label Image

120 mg (Propranolol Hydrochloride Extended Release Capsule 8)

Label for Propranolol Hydrochloride Extended-Release Capsules, USP 120 mg by Lannett Company, Inc. The label states the product is an extended-release oral capsule containing 120 mg propranolol hydrochloride. It includes storage instructions, child safety warnings, manufacturer information, and a package count of 100 capsules. The product is marked Rx only.*

FDA Label Image

160 mg (Propranolol Hydrochloride Extended Release Capsule 9)

Label for Propranolol Hydrochloride Extended-Release Capsules, USP 160 mg by Lannett Company, Inc. The label indicates the product contains 100 capsules in extended-release oral capsule form. It includes storage and handling instructions, dosage caution, and manufacturer details from Yichang Humanwell Oral Solid Dosage Plant, China.*

* 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.