Doxepin Hydrochloride
Product Images NDC 21695-943

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Doxepin Hydrochloride (NDC 21695-943). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rebel Distributors Corp, 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 (F6ffd0d8 3451 425e 921e Faae1c1b8ad3 01)

Chemical structure diagram of doxepin hydrochloride, displaying the molecular framework including two aromatic rings connected by an oxygen-containing ring and a side chain with nitrogen, representing the hydrochloride form.*

FDA Label Image

Doxepin HCl 10mg (F6ffd0d8 3451 425e 921e Faae1c1b8ad3 02)

Packaging label for Doxepin Hydrochloride 10 mg capsules, containing 30 capsules per bottle. The label shows the product ID PD044130 and states that each capsule is a hard-shell gelatin capsule with a buff opaque cap and body, axially printed with "MYLAN" over "1049." It is labeled as RX only and manufactured by Mylan Pharmaceuticals Inc., Morgantown, WV, with packaging by Physician Partner, Thousand Oaks, CA.*

FDA Label Image

Doxepin HCl 50mg (F6ffd0d8 3451 425e 921e Faae1c1b8ad3 03)

Label for Doxepin Hydrochloride 50 mg capsules, with a package count of 30 capsules. The label specifies each capsule contains Doxepin HCl USP equivalent to 50 mg of Doxepin. It includes manufacturer details for Mylan Pharmaceuticals Inc., Morgantown, WV, and packaging by Physician Partner in Thousand Oaks, CA. The label features lot, expiration, and product ID information with instructions for controlled room temperature storage and child safety.*

* 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.