Carvedilol Tablet, Film Coated
Product Images NDC 51655-030

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Carvedilol (NDC 51655-030). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, Llc, 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

Label (51655 030 25 Master Bottle Label Approval Rev A 04 22)

This is a description of Carvedilol tablets, USP with 12.5mg dosage. The NDC (National Drug Code) for the product is 51655-030-25. Each tablet contains Carvedilol USP. The tablets are repackaged and distributed by Northwind Pharmaceuticals in Indianapolis, IN. The lot number for the repackaged product is 0000000000. The tablets should be stored at 20°C - 25°C and kept away from moisture. The package contains 60 tablets and should be kept out of the reach of children. Further dosage information can be found in the included package insert. S/N and GTIN are also included in the description.*

FDA Label Image

Structured Formula For Carvedilol (B1fa8af3 9789 45d2 8b77 A53935c52b49 01)

FDA Label Image

Carvedilol Tablets (B1fa8af3 9789 45d2 8b77 A53935c52b49 02)

FDA Label Image

Carvedilol Tablets (B1fa8af3 9789 45d2 8b77 A53935c52b49 03)

FDA Label Image

Structured Formula For Carvedilol (B1fa8af3 9789 45d2 8b77 A53935c52b49 04)

FDA Label Image

Structured Formula For Carvedilol (B1fa8af3 9789 45d2 8b77 A53935c52b49 05)

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