Sentravil Pm-25
Product Images NDC 68405-053

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sentravil Pm-25 (NDC 68405-053). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Physician Therapeutics 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

Amitriptyline (Amitriptyline)

Label for Amitriptyline 25mg tablet, showing manufacturer as Sandoz and lot number AYL207S. The label indicates a quantity of 30 tablets, with an expiration date of 03/10. It references comparison to Elavil with manufacturer NDC 00781-1487-10 and advises to take as directed by a doctor or see the outsert for usual dosage information. The label includes multiple small repeated sections with the same product information and barcodes.*

FDA Label Image

Amitriptyline Formula (Amitriptyline Formula)

Chemical structure diagram of the active ingredient in Sentravil PM-25, showing the molecular formula C20H23N with hydrochloride (HCl) and molecular weight 313.87.*

FDA Label Image

Sentra Pm (Sentrapm)

This label for Sentravil PM-25 by Physician Therapeutics provides directions for use, stating it is for adults only and should be taken under physician supervision at bedtime. It details its role in the dietary management of sleep disorders, storage instructions, and a warning to keep out of reach of children. The ingredient list includes a proprietary amino acid formulation and other components. The product contains 60 capsules per package.*

FDA Label Image

Sentravil Pm-25 (Sentravilpm 25)

Packaging label for Sentravil PM-25 by Physician Therapeutics LLC. It features Sentra PM 60 capsules and Amitriptyline 25 mg 30 tablets in a co-pack. The label includes physician authorization and Rx only notice, along with the NDC number 68405-053-26 for this co-pack.*

* 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.