Amitriptyline Hydrochloride
Product Images NDC 67296-0388

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Amitriptyline Hydrochloride (NDC 67296-0388). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

67296-0388 (Doc20161118100245 001)

This is information for a medication called Amitriptyline HCL that is available in 25mg tablets. There are two different tablet quantities presented: 30 tablets with a Lot number of 169600 1 and expiration date of 07/10, and 42 tablets with a Lot number of 169601 1 and expiration date of 09/10. The medication should be stored at a controlled room temperature of 20-25C (68-77F). The manufacturer is Sandoz Inc. located in Princeton, NJ and it is distributed by Redpharm Drug in Eden Prairie, MN. The usual adult dosage is not provided; it should be referenced through the package insert.*

FDA Label Image

Amitriptyline 25mg (Doc20171213141308 001)

This is a description of a medication called Amitriptyline HCL in the form of 15 tablets, each containing 25mg of the medication. The medication can only be obtained with a prescription (Rx Only). The medication is manufactured by Sandoz Inc. and distributed by Redpharm Drug in Eden Prairie, MN. The lot number is HD3649 with an expiration date of 04/20. The medication should be stored between 20-25°C (68-77°F). There is additional information on the dosage in the package insert. The NDC number for this product is 67296-0388-3.*

* 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.