Carvedilol Phosphate Capsule, Extended Release
Product Images NDC 63629-9634

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 Carvedilol Phosphate (NDC 63629-9634). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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 (Carvedilol 1)

Structure (Carvedilol 1)
Chemical structure of carvedilol phosphate showing its molecular arrangement including aromatic rings and functional groups, with annotations for phosphate and water molecules.*
FDA Label Image

Figure (Carvedilol 2)

Figure (Carvedilol 2)
Two line graphs illustrate changes in systolic and diastolic blood pressure (SBP and DBP) over 24 hours after a morning dose of Carvedilol Phosphate extended-release capsules at 20 mg, 40 mg, and 80 mg strengths. The graphs plot time on the x-axis and blood pressure change on the y-axis, with smoothed trend lines for each dosage.*
FDA Label Image

Label (Lbl636299634)

Label (Lbl636299634)
Label for Carvedilol Phosphate extended-release capsules, 40 mg, oral dosage form. The label displays the NDC 63629-9634-1, quantity of 30 capsules, and includes storage instructions to keep between 20° to 25°C with temporary excursions allowed from 15° to 30°C. It also advises dispensing in a tight, light-resistant container. The label shows the product is repackaged by Bryant Ranch Prepack in Burbank, CA, and manufactured by Frontida BioPharm Inc. Barcodes and the BRP Pharmaceuticals logo are present.*

* 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.