Amitriptyline Hydrochloride Tablet, Film Coated
Product Images NDC 80425-0285

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Amitriptyline Hydrochloride (NDC 80425-0285). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Pharmacy Of Tennessee, 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 1 (Amitriptyline HCl 80425 0285 01)

Amitriptyline Hydrochloride 25 mg tablet carton from Advanced Rx Pharmacy of Tennessee, LLC. The label includes directions to store at 20-25°C (68-77°F), a comparison to ELAVIL, NDC 80425-0285-01, lot number 30AMT25924, and expiration date 9/30/2024. The package size is 30 tablets.*

FDA Label Image

Label 2 (Amitriptyline HCl 80425 0285 02)

Label for Amitriptyline HCl 25 mg tablet manufactured by Advanced Rx Pharmacy of Tennessee, LLC, NDC 80425-0285. The label includes storage instructions, a comparison to Elavil, expiration date 3/30/2023, barcode, and lot number information.*

FDA Label Image

Label 3 (Amitriptyline HCl 80425 0285 03)

Amitriptyline Hydrochloride 25 mg tablet label from Advanced Rx Pharmacy of Tennessee, LLC. The label indicates a count of 90 tablets and includes a comparison to ELAVIL. It displays the product NDC 80425-0285-03 and source NDC 29300-0420-01, with storage instructions at 20-25°C (68-77°F) and an expiration date of 3/30/2023.*

FDA Label Image

Description (Description)

Chemical structure diagram of amitriptyline hydrochloride, showing its tricyclic ring system and side chain with a dimethylamino group.*

FDA Label Image

Logo (Logo)

* 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.