Amitriptyline Hydrochloride Tablet, Film Coated
Product Images NDC 71335-1256

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 Amitriptyline Hydrochloride (NDC 71335-1256). 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 (Amitriptyline 01)

Structure (Amitriptyline 01)
Chemical structure diagram of amitriptyline hydrochloride, showing the tricyclic core structure with an attached side chain including a nitrogen atom bonded to two methyl groups and a hydrochloride indicated.*
FDA Label Image

Label (Lbl713351256)

Label (Lbl713351256)
Label for Amitriptyline Hydrochloride Tablets USP 50 mg by Bryant Ranch Prepack. The label shows NDC 71335-1256-01, package size of 100 tablets, and a red boxed area highlighting the 50 mg strength. Storage instructions and drowsiness warning are also visible. Manufactured by Florida Biopharm Inc.*
FDA Label Image

Label (Lbl7133512562)

Label (Lbl7133512562)
Label for Amitriptyline Hydrochloride 50 mg tablets by Bryant Ranch Prepack. The label compares this product to Elavil 50 mg tablets from Frontida BioPharm, Inc. The packaging indicates a quantity of 100 tablets, with a lot number 1523487 and an NDC of 71335-1256-1. It includes storage instructions for room temperature (20°-25°C) and a warning about potential drowsiness and keeping drugs out of reach of children.*

* 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.