Propranolol Hydrochloride Tablet
Product Images NDC 60687-609

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Propranolol Hydrochloride (NDC 60687-609). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

10 mg Propranolol Hydrochloride Tablet Blister (10 mg Blister)

Label sheet for Propranolol Hydrochloride 10 mg oral tablets by American Health Packaging showing multiple identical barcode labels. Each label includes the drug name, strength, dosage form, barcode, and labeler address in Columbus, Ohio. Space is provided for expiration date and lot number.*

FDA Label Image

10 mg Propranolol Hydrochloride Tablets Carton (10 mg Carton)

Label for Propranolol Hydrochloride Tablets, USP, 10 mg strength, packaged as 100 tablets (10 x 10) for oral use. The label shows the NDC 60687-587-01, indicates prescription only, and is distributed by American Health Packaging, Columbus, Ohio. Additional storage and safety instructions are included.*

FDA Label Image

20 mg Propranolol Hydrochloride Tablet Blister (20 mg Blister)

Labels for Propranolol Hydrochloride oral tablets by American Health Packaging, showing strength of 20 mg. Each label includes the proprietary and generic name, dosage form (tablet), strength, barcode, and spaces for lot number and expiration date. One label shows 10 mg strength.*

FDA Label Image

20 mg Propranolol Hydrochloride Tablets Carton (20 mg Carton)

Propranolol Hydrochloride 20 mg tablets in a package of 100 tablets (10 x 10) by American Health Packaging. The label displays the NDC number 60687-598-01 and includes usage and storage instructions as well as protection and safety information. The product is Rx only and intended for oral use.*

FDA Label Image

40 mg Propranolol Hydrochloride Tablet Blister (40 mg Blister)

Labels for Propranolol Hydrochloride tablets, USP, 40 mg strength, oral dosage form. Each label displays the product name, strength, barcode, expiration and lot number placeholders, and is labeled by American Health Packaging, Columbus, Ohio. The layout includes multiple identical labels on a single sheet intended for packaging.*

FDA Label Image

40 mg Propranolol Hydrochloride Tablets Carton (40 mg Carton)

Propranolol Hydrochloride 40 mg tablets label from American Health Packaging. The label indicates 100 tablets (10x10) per package, with the National Drug Code (NDC) 60687-609-01. It includes storage instructions, protection from light, and usage precautions. The tablets are oral dosage form and prescription only.*

FDA Label Image

Ahp58701

Propranolol Hydrochloride 10 mg oral tablet shown in front and back views. The tablet is round, light peach-colored, scored with imprint 'I' above a score line and '155' below it. This tablet is a prescription drug labeled by American Health Packaging.*

FDA Label Image

Ahp59801

Propranolol Hydrochloride 10 mg oral tablet, round and blue, scored on one side with imprint 'I 157' and plain on the other side. Manufactured by American Health Packaging.*

FDA Label Image

Ahp60901

Propranolol Hydrochloride 10 mg oral tablet, round, light green, with imprint code 'I 159' on one side and plain on the other. Manufactured by American Health Packaging.*

FDA Label Image

Structural Formula (Structure)

Chemical structure of Propranolol Hydrochloride depicted with two fused aromatic rings and attached functional groups including hydroxyl, ether, and amine groups along with the hydrochloride (HCl) component.*

* 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.