Atropine Sulfate
Product Images NDC 0641-6006

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Atropine Sulfate (NDC 0641-6006). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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

Structural Formula (Atropine Sulfate Injection Usp 1)

Chemical structure diagram of atropine sulfate showing its molecular arrangement, including multiple ring structures and sulfate and water components as indicated.*

FDA Label Image

West-ward Logo (Atropine Sulfate Injection Usp 2)

Label for Atropine Sulfate Injection, USP 8 mg per 20 mL (0.4 mg/mL) by Hikma Pharmaceuticals USA Inc. The label states the product is for intramuscular (IM), intravenous (IV), or subcutaneous (SC) use, packaged in a 20 mL multiple dose vial. Additional text includes formulation details and storage instructions.*

FDA Label Image

Atropine Sulfate Injection, Usp 8 mg/20 mL (0.4 mg/ml) 20 mL Multiple Dose Vial (Atropine Sulfate Injection Usp 3)

Atropine Sulfate Injection, USP 8 mg per 20 mL (0.4 mg/mL) vial label by Hikma Pharmaceuticals USA Inc. The label indicates the product is for intramuscular, intravenous, or subcutaneous use and comes in a package of 10 multiple dose vials, each 20 mL. Additional details include NDC 0641-6006-10, Rx only, storage instructions, and ingredient concentrations.*

FDA Label Image

Atropine Sulfate Injection, Usp 8 mg/20 mL (0.4 mg/ml) 10 X 20 mL Multiple Dose Vials (Atropine Sulfate Injection Usp 4)

A label showing a QR code and alphanumeric identifiers including GTIN, serial number (SN), expiration date (EXP), and lot number (LOT). The label corresponds to Atropine Sulfate by Hikma Pharmaceuticals USA Inc., product NDC 0641-6006.*

* 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.