Amitriptyline Hydrochloride Tablet, Film Coated
Product Images NDC 70710-1228

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Amitriptyline Hydrochloride (NDC 70710-1228). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Pharmaceuticals Usa 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.

FDA Label Image

Structure (Ffef783d 68b3 4490 A0a3 3643af89e541 01)

Chemical structure of Amitriptyline Hydrochloride, showing the molecular arrangement including two aromatic rings, a three-ring central fused structure, and an attached side chain with nitrogen. The formula C20H23N · HCl and molecular weight 313.87 are displayed.*

FDA Label Image

Amitriptyline Hydrochloride Tablets, Usp (Ffef783d 68b3 4490 A0a3 3643af89e541 02)

Label for Amitriptyline Hydrochloride Tablets, USP 10 mg, film-coated oral tablets. The label states 100 tablets per container, prescription only, manufactured by Zydus Pharmaceuticals USA Inc. Instructions note child-resistant packaging and storage between 20°C to 25°C. It includes a barcode, the NDC number 70710-1225-1, and instructions for pharmacists to dispense medication guides separately.*

FDA Label Image

Amitriptyline Hydrochloride Tablets, Usp (Ffef783d 68b3 4490 A0a3 3643af89e541 03)

Amitriptyline Hydrochloride Tablets USP 25 mg film-coated oral tablets label. The label includes the strength (25 mg), package count (100 tablets), prescription status (Rx only), and instructions for pharmacists to dispense the medication guide. The label also shows storage instructions, manufacturer Cadila Healthcare Ltd., India, and distributor Zydus Pharmaceuticals USA Inc. A barcode and the NDC number 70710-1226-1 are present.*

FDA Label Image

Amitriptyline Hydrochloride Tablets, Usp (Ffef783d 68b3 4490 A0a3 3643af89e541 04)

Amitriptyline Hydrochloride Tablets, USP 50 mg film-coated oral tablets packaging label from Zydus Pharmaceuticals USA Inc. The label indicates 100 tablets per package, prescription use only, with medication guide and storage instructions included.*

FDA Label Image

Amitriptyline Hydrochloride Tablets, Usp (Ffef783d 68b3 4490 A0a3 3643af89e541 05)

Amitriptyline Hydrochloride Tablets USP 75 mg film-coated oral tablets label. The label states the package contains 100 tablets and is for prescription use only. Instructions include pharmacist dispensing medication guide separately. The label shows storage conditions, manufacturer Cadila Healthcare Ltd. India, and distributor Zydus Pharmaceuticals USA Inc.*

FDA Label Image

Amitriptyline Hydrochloride Tablets, Usp (Ffef783d 68b3 4490 A0a3 3643af89e541 06)

Label for Amitriptyline Hydrochloride Tablets, USP 100 mg film-coated tablets by Zydus Pharmaceuticals USA Inc. The packaging contains 100 tablets intended for oral use. The label includes storage instructions, dosage form, manufacturer and distributor information, plus a pharmacist note to dispense a separate Medication Guide. The package is indicated as child-resistant and for prescription use only.*

FDA Label Image

Amitriptyline Hydrochloride Tablets, Usp (Ffef783d 68b3 4490 A0a3 3643af89e541 07)

The label for Amitriptyline Hydrochloride Tablets, USP, 150 mg film-coated oral tablets, manufactured by Zydus Pharmaceuticals USA Inc. The label states a package count of 100 tablets and includes dosage and storage instructions, warnings about child resistance, and distributor information. The label includes a barcode and a purple and white color scheme.*

* 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.