Structure (Trazodone 02)
Trazodone Hydrochloride Tablet, Film Coated
Product Images NDC 57664-014
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Trazodone Hydrochloride (NDC 57664-014). 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.
Product Images & Figures Index
Trazodone-04 (Trazodone 04)
Each tablet of TraZODONE Hydrochloride Tablets USP contains 50mg of 1raZODONE HCI, USP. The package insert should be consulted for dosage information. These tablets should be kept in a tightly closed, light-resistant container at room temperature. The medication guide should be dispensed to each patient. This medication should be kept out of reach of children. The tablets are distributed by Sun Pharmaceutical Industries, Inc. and manufactured by Sun Pharmaceutical Industries Ltd. The expiry date should be overprinted in MM/YYYY format.*
Trazodone-05 (Trazodone 05)
Each tablet contains 100 mg of trazodone HCI, USP. The package insert should be consulted for dosage information. The tablets should be stored at room temperature in a tightly sealed and light-resistant container. Excursions are allowed between 15°C to 30°C. The medication should be kept out of reach of children. Pharmacists are advised to provide patients with a medication guide. The tablets are distributed by Sun Pharmaceutical Industries, Inc., and manufactured by Sun Pharmaceutical Industries Ltd. The expiration date is to be overprinted in MM/YYYY format. NDC 57664-026-72.*
Trazodone-06 (Trazodone 06)
This is a medication named Trazodone Hydrochloride. Each tablet contains 150 mg of the medication. The recommended dosage information is available in the package insert. The medication should be kept in a light-resistant container at room temperature i.e., 20°C to 25°C (68F to 77°F) with permitted excursions between 15°C to 30°C (59°F to 86°F). The medication guide is available on https://www.sunpharma.com/usa/products. The medication should be kept away from the reach of children. The expiry date needs to be overprinted in MMYYYY. The medicine can only be dispensed with the prescription.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
