Acetazolamide Injection, Powder, Lyophilized, For Solution
Product Images NDC 68083-661

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Acetazolamide (NDC 68083-661). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gland Pharma Limited, 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

Acetazolamide-spl-carton (Acetazolamide Spl Carton)

Packaging label for Acetazolamide injection, USP, 500 mg/vial, powder, lyophilized, for intravenous use. The label shows the product name in uppercase and lowercase letters, strength, and dosage form. It states single-dose vial and provides storage and reconstitution instructions. Manufactured by Gland Pharma Limited, with NDC 68083-661-01.*

FDA Label Image

Acetazolamide-spl-container (Acetazolamide Spl Container)

Label for Acetazolamide for Injection, USP 500 mg/vial, lyophilized powder for intravenous use. The label states it is a single-dose vial containing acetazolamide sodium equivalent to 500 mg. Storage instructions include keeping the vial at 20° to 25°C before reconstitution and refrigeration at 2° to 8°C after reconstitution, with use within 12 hours. Manufactured by Gland Pharma Limited, Hyderabad, India. The label also includes a barcode and placeholders for lot number and expiration date.*

FDA Label Image

Acetazolamide-structure (Acetazolamide Structure)

Chemical structure of acetazolamide, showing a sulfonamide group attached to a heterocyclic ring with additional functional groups including an amide and methyl group.*

* 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.