Atropine Sulfate Injection
Product Images NDC 0641-6251

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Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Atropine Sulfate (NDC 0641-6251). 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

Atropine Sulfate Structural Formula (Atropine Sulfate Injection Usp Anda 1)

FDA Label Image

Atropine Sulfate Injection, Usp 8 mg Per 20 mL Container Label (Atropine Sulfate Injection Usp Anda 2)

Atropine Sulfate Injection, Usp 8 mg Per 20 mL Container Label (Atropine Sulfate Injection Usp   Anda 2)
Atropine Sulfate Injection, USP with NDC code 0641-6251-01 is a sterile solution containing 8 mg Atropine sulfate per 20 mL. It is suitable for intravenous, intramuscular, subcutaneous, intraosseous, or endotracheal use. The solution is adjusted with sulfuric acid to achieve a pH of 3.5 (30 to 35). Each mL contains 0.4 mg/mL Atropine sulfate, equivalent to 0.33 mg of atropine. The package comes with 20 single-dose vials. The solution contains benzyl alcohol and sodium chloride, and the instructions recommend referring to the prescribing information for proper dosage. After initial use, the package should be stored at 20°C to 25°C and discarded within two hours to prevent contamination. It is distributed by Hikma Pharmaceuticals and should be used with caution and under medical supervision.*
FDA Label Image

Atropine Sulfate Injection, Usp 8 mg Per 20 mL Carton Label (Atropine Sulfate Injection Usp Anda 3)

Atropine Sulfate Injection, Usp 8 mg Per 20 mL Carton Label (Atropine Sulfate Injection Usp   Anda 3)
Atropine Sulfate Injection is a medicine with the National Drug Code (NDC) 0641-6251-10. It is a multiple-dose vial that contains 8mg per 20mL (0.4mg/mL) of Atropine Sulfate, with benzyl alcohol and sodium chloride. It can be used intravenously, intramuscularly, subcutaneously, intraosseously, or endotracheally. Its pH level is 3.5 (3010 3.8), and after the initial use, it should be stored between 20°C to 25°C (68°F to 77°F) and discarded within 24 hours. The usual dosage is indicated in the prescribing information. It is manufactured by Hikma in Berkeley Heights, New Jersey.*
FDA Label Image

Representative Serialization Image (Atropine Sulfate Injection Usp Anda 4)

Representative Serialization Image (Atropine Sulfate Injection Usp   Anda 4)
This is a product label that includes a GTIN (Global Trade Item Number) of 0301234567896, a SN (Serial Number) of 1234567890123, an expiration date of MMMYYYY, and a lot number of ABCDE12345. The product details are not specified.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.