Amitriptyline Hydrochloride Tablet, Coated
Product Images NDC 69367-390

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Amitriptyline Hydrochloride (NDC 69367-390). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Westminster Pharmaceuticals, 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

Chemical Structure (Amitriptyline 01)

Chemical Structure (Amitriptyline 01)
Chemical structure diagram of Amitriptyline Hydrochloride showing the molecular framework with two aromatic rings, a seven-membered central ring, and a side chain containing nitrogen and methyl groups, labeled with HCl indicating the hydrochloride salt form.*
FDA Label Image

Principal Display Panel (10 mg Tablet Bottle Label)

Principal Display Panel (10 mg Tablet Bottle Label)
Amitriptyline Hydrochloride Tablets, USP 10 mg coated oral tablets packaging label, containing 100 tablets. The label shows the drug name with strength prominently, includes storage and handling instructions, prescription dispensing information, and manufacturing details for Westminster Pharmaceuticals, LLC. The label also features a barcode and the NDC number 69367-388-01.*
FDA Label Image

Principal Display Panel (25 mg Tablet Bottle Label)

Principal Display Panel (25 mg Tablet Bottle Label)
Amitriptyline Hydrochloride Tablets USP 25 mg coated tablets label. The label shows 100 tablets manufactured by Westminster Pharmaceuticals, LLC. It includes storage instructions, dosage information, and manufacturer details from Zhejiang Jingxin Pharmaceutical Co., Ltd, China. The label displays the NDC 69367-389-01 and notes child-resistant packaging.*
FDA Label Image

Principal Display Panel (50 mg Tablet Bottle Label)

Principal Display Panel (50 mg Tablet Bottle Label)
Label of Amitriptyline Hydrochloride Tablets USP 50 mg, coated oral tablets, supplied in a bottle of 100 tablets. The label shows the product name, strength, dosing guidance to consult prescribing info, manufacturer Zhejiang Jingxin Pharmaceutical Co., Ltd. in China, and labeler Westminster Pharmaceuticals, LLC, Nashville, TN. Storage instructions and child-resistant packaging information are included.*
FDA Label Image

Principal Display Panel (75 mg Tablet Bottle Label)

Principal Display Panel (75 mg Tablet Bottle Label)
Label for Amitriptyline Hydrochloride Tablets, USP 75 mg, coated oral tablets in a package of 100 tablets. The label indicates the labeler as Westminster Pharmaceuticals, LLC and includes storage instructions, child-resistant packaging information, and manufacturer details from Zhejiang Jingxin Pharmaceutical Co., Ltd. A barcode and NDC number 69367-391-01 are also shown.*
FDA Label Image

Principal Display Panel (100 mg Tablet Bottle Label)

Principal Display Panel (100 mg Tablet Bottle Label)
Amitriptyline Hydrochloride Tablets, USP 100 mg coated tablets label. The label indicates a package of 100 tablets, manufactured by Zhejiang Jingxin Pharmaceutical Co., Ltd. for Westminster Pharmaceuticals, LLC. It includes dosage information, storage instructions, and a barcode on a white and gold background with maroon accents.*
FDA Label Image

Principal Display Panel (150 mg Tablet Bottle Label)

Principal Display Panel (150 mg Tablet Bottle Label)
Amitriptyline Hydrochloride Tablets USP 150 mg coated tablets label. The label states a pack size of 100 tablets and notes the product is Rx only. Manufactured by Zhejiang Jingxin Pharmaceutical Co., Ltd (China) for Westminster Pharmaceuticals, LLC. The label includes storage instructions, a medication guide URL, and a barcode.*

* 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.