Chlordiazepoxide And Amitriptyline Hydrochloride
Product Images NDC 42571-303

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Chlordiazepoxide And Amitriptyline Hydrochloride (NDC 42571-303). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Micro Labs Limited, 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

Chlorodiazepoxideamitriptlyne-10label.jpg (Chlorodiazepoxideamitriptlyne 10label)

This text is a description of a medication containing chlordiazepoxide and amitriptyline. The medication comes in film-coated tablets with 10mg of chlordiazepoxide and 27.98mg of amitriptyline hydrochloride. The tablets should be dispensed in a tight, light-resistant container with a child-resistant closure and stored at controlled room temperature. Usual adult dosage information should be referred to for each patient. It is manufactured by Micro Labs USA, Inc. in Somerset, NJ.*

FDA Label Image

Chlorodiazepoxideamitriptlyne-5label.jpg (Chlorodiazepoxideamitriptlyne 5label)

This appears to be the label of a medication (Chlordiazepoxide and Amitriptyline Hydrochloride Tablets) with each film-coated tablet containing 5 mg of chlordiazepoxide and 14 mg of amitriptyline hydrochloride, equivalent to 12.5 mg of amitriptyline. It is recommended to dispense in a secure container to prevent children's reaching the medicine. The standard adult dosage is found in the prescribing information. It provides the NDC code: 42571-302-01, which is for "Rx only," and that it is manufactured by Micro Labs USA, Inc. The artwork code and the pharmacist's information are also included.*

* 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.