Acetazolamide Tablet
Product Images NDC 68071-3632

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Acetazolamide (NDC 68071-3632). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare 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 (C087a4a4 Dd45 4b06 8b7c 76be61a8c063 01)

Image (C087a4a4 Dd45 4b06 8b7c 76be61a8c063 01)
Chemical structure diagram of acetaZOLAMIDE, showing its molecular arrangement with nitrogen, sulfur, oxygen atoms, and functional groups as part of the compound.*
FDA Label Image

Container Label 125 mg (C087a4a4 Dd45 4b06 8b7c 76be61a8c063 02)

Container Label 125 mg (C087a4a4 Dd45 4b06 8b7c 76be61a8c063 02)
Label for acetaZOLAMIDE Tablets, USP 125 mg oral tablets. This prescription drug package contains 100 tablets. The label includes storage instructions, child-resistant packaging notice, and manufacturer details: Zydus Lifesciences Ltd. and distributor Viona Pharmaceuticals Inc. A barcode and NDC 72578-149-01 are also visible.*
FDA Label Image

Container Label 250 mg (C087a4a4 Dd45 4b06 8b7c 76be61a8c063 03)

Container Label 250 mg (C087a4a4 Dd45 4b06 8b7c 76be61a8c063 03)
Label for acetaZOLAMIDE Tablets, USP 250 mg, oral tablet form. The label indicates a package size of 100 tablets, with Rx only status. The labeler mentioned is Viona Pharmaceuticals Inc., and the manufacturer is Zydus Lifesciences Ltd., India. Storage instructions and warnings are included, along with a barcode and NDC 72578-150-01.*

* 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.