Penicillamine Capsule
Product Images NDC 71205-916

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Penicillamine (NDC 71205-916). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

71205-916-00 (Pencillamine 100s Label Jpg)

Label for Penicillamine 250 mg capsules, supplied in a 100-count package by Proficient Rx LP. The label states each capsule contains 250 mg of penicillamine USP. It includes storage instructions and manufacturer info for Granules Pharmaceuticals Inc., Chantilly, VA. The label features barcodes, QR codes, and dosage form details.*

FDA Label Image

Pencillamine-configuration-jpg (Pencillamine Configuration Jpg)

Chemical structure diagram showing the molecular configuration of Penicillamine, the active ingredient in this product. The structure includes labeled angles and notation related to its stereochemistry and chemical environment.*

FDA Label Image

Pencillamine-structure-jpg.jpg (Pencillamine Structure Jpg)

Chemical structure of penicillamine, showing its molecular arrangement with amino, thiol, carboxyl, and methyl groups attached to the central carbon structure.*

FDA Label Image

Penicillamine Reaction.jpg.jpg.jpg

Chemical reaction diagram showing the interactions and disulfide bonding between cystine (CSSC), deprotonated cysteine (CS'), penicillamine disulfide (PSSP), deprotonated penicillamine sulfhydryl (PS'), and penicillamine-cysteine mixed disulfide (CSSP). It includes definitions of each chemical abbreviation involved in these reactions.*

* 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.