Penicillamine Tablet
Product Images NDC 70748-153

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Penicillamine (NDC 70748-153). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin Pharmaceuticals, 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

Image 01 (Cd2c8cf5 209b 4473 Bf16 Cd231f024009 01)

A scientific data table showing optical rotation notation with angular values and chemical conditions, including "[a] 25° = -62.5° ± 2.0° (C = 1, 1N NaOH) D". This appears to be related to the physical characterization of the compound.*

FDA Label Image

Image 02 (Cd2c8cf5 209b 4473 Bf16 Cd231f024009 02)

Chemical structure of penicillamine showing its molecular formula with functional groups including a thiol (-SH), carboxyl (-COOH), amino (-NH2), and methyl (CH3) substituents attached to the carbon backbone.*

FDA Label Image

Image 03 (Cd2c8cf5 209b 4473 Bf16 Cd231f024009 03)

Chemical structure diagram depicting a series of chemical equilibrium reactions involving molecular species represented by abbreviations such as CSSC, PS', CS', CSSP, PSSP, and others. The image shows three reversible reaction equations illustrating the interchange between these species.*

FDA Label Image

Image 04 (Cd2c8cf5 209b 4473 Bf16 Cd231f024009 04)

Label for Penicillamine Tablets, USP (Titrable Tablets) showing strength of 250 mg per tablet. The label specifies the product is available as 100 tablets per container. Manufactured for Lupin Pharmaceuticals, Inc. and made by Lupin Limited in India. Storage instructions and prescription-only status are also displayed.*

* 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.