Felodipine Tablet, Extended Release
Product Images NDC 13668-133

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Felodipine (NDC 13668-133). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Torrent Pharmaceuticals Limited, 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

Str (Felodipine Figure 01)

Chemical structure of Felodipine, showing its molecular configuration with distinctive groups and atoms, including chlorine and methoxy substituents, corresponding to the active ingredient in Felodipine tablets.*

FDA Label Image

Logo (Felodipine Figure 02)

FDA Label Image

2.5 (Felodipine Figure 03)

Label for Felodipine Extended-Release Tablets USP 2.5 mg in a package of 30 tablets. The label includes storage instructions and warnings to keep drugs out of reach of children. The product is manufactured by Torrent Pharmaceuticals Limited and labeled for prescription use only. A barcode and lot number are also visible.*

FDA Label Image

5 (Felodipine Figure 04)

Label for Felodipine Extended-Release Tablets, USP 5 mg, showing a 30-tablet package. The label states each film-coated extended-release tablet contains 5 mg of felodipine. It includes storage instructions, a caution to keep out of reach of children, and manufacturer information for Torrent Pharmaceuticals Limited, India, and Torrent Pharma Inc., NJ. The label also features barcode and Rx only designation.*

FDA Label Image

10 (Felodipine Figure 05)

Label for Felodipine Extended-Release Tablets, USP 10 mg by Torrent Pharmaceuticals Limited. The label states the package contains 30 extended-release tablets. It includes storage instructions, a warning to keep out of reach of children, and a note to see accompanying prescribing information. The label also features the NDC 13668-134-30, barcodes, and specifies 'Rx only.'*

* 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.