Atropine Sulfate Solution
Product Images NDC 70069-631

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Atropine Sulfate (NDC 70069-631). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Somerset Therapeutics, Llc, 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

Structure (7a8a5552 Fe21 4d36 8396 B7c99f41b4c4 01)

Chemical structure of atropine sulfate showing the molecular arrangement including a tropane ring, ester linkage, and phenyl group with sulfate and water molecules indicated.*

FDA Label Image

Container (0.4mg)

Atropine Sulfate Injection, USP 0.4 mg/mL solution for intravenous use in a 1 mL single-dose vial. The label indicates it is manufactured for Somerset Therapeutics, LLC, Somerset, NJ, and made in India. Storage instructions recommend 20° to 25°C with permitted excursions between 15° and 30°C. The label includes an NDC code and barcode.*

FDA Label Image

Carrton (0.4mg)

Packaging label for Atropine Sulfate Injection, USP 0.4 mg/mL solution for intravenous use. The label indicates a pack of 25 single-dose 1 mL vials by Somerset Therapeutics, LLC, with storage instructions and manufacturing details shown. Barcode and prescription-only status are also present.*

FDA Label Image

Container (1 mg)

Label for Atropine Sulfate Injection, USP 1 mg/mL solution for intravenous use. The product is a 1 mL single-dose vial. Label indicates it is prescription only and instructs to discard unused portion. Manufactured for Somerset Therapeutics, LLC, Somerset, NJ, and made in India. Storage instructions and barcode are also visible.*

FDA Label Image

Carton (1mg)

Atropine Sulfate Injection, USP 1 mg/mL intravenous solution label for 25 single-dose 1 mL vials by Somerset Therapeutics, LLC. The label includes drug strength, route, lot and expiration blank area, storage instructions, and manufacturer details. The package features barcodes and NDC 70069-641-25.*

* 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.