Carvedilol Tablet, Film Coated
Product Images NDC 72789-411

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Carvedilol (NDC 72789-411). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx 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

Structured Formula For Carvedilol (2c528763 Eac4 4001 A828 95a981ad29b1 01)

FDA Label Image

Carvedilol Tablets (2c528763 Eac4 4001 A828 95a981ad29b1 02)

FDA Label Image

Carvedilol Tablets (2c528763 Eac4 4001 A828 95a981ad29b1 03)

FDA Label Image

Structured Formula For Carvedilol (2c528763 Eac4 4001 A828 95a981ad29b1 04)

FDA Label Image

Structured Formula For Carvedilol (2c528763 Eac4 4001 A828 95a981ad29b1 05)

FDA Label Image

72789411 Label (72789411)

72789411 Label (72789411)
This is a description of Carvedilol medication in the form of 3.125mg tablets. The package includes 90 tablets with the NDC number 72789-411-90. It is USP-certified and has an expiration date of September 2025. Patients are advised to contact their doctor regarding side effects and can report any issues to the FDA at 1-800-FDA-1088. The tablets are to be taken multiple times a day as per medical advice.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.