Structure (Carvedilol 1)
Carvedilol Phosphate Capsule, Extended Release
Product Images NDC 57664-663
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 Phosphate (NDC 57664-663). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Sun Pharmaceutical Industries, 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.
Figure 5 (Carvedilol 2)
Change in SBP and DBP (measured in mmHg) at different time points after morning dosage. The data seems to have been smoothed using a locally weighted regression smoothing methodology.*
Principal Display Panel (10mg)
This is a description for a prescription medication called Carvedilol Phosphate, which is presented in capsules form. The medication is designed for once-a-day dosing with 30 capsules in a pack. The capsules are extended-release and intended for prescription use only. The rest of the text seems to be jumbled and does not provide any useful information.*
Principal Display Panel (20mg)
This is the label from a prescription drug, Carvedilol Phosphate, which is available in the form of extended-release capsules to be taken once a day. The package contains 30 capsules and can only be dispensed with a valid prescription.*
Principal Display Panel (40mg)
This is a description for Carvedilol Phosphate Capsules. The drug is taken once a day and comes in a bottle containing 30 extended-release capsules. The National Drug Code (NDC) for the drug is 57664-665. It is a prescription medication labeled as Rx only.*
Principal Display Panel (80mg)
* 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.
