Atropine Solution/ Drops
Product Images NDC 60219-1749

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Atropine (NDC 60219-1749). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Ny 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

Ab (Atropine Sulfate Ophthalimic Solution 1)

Ab (Atropine Sulfate Ophthalimic Solution 1)
Chemical structure of atropine sulfate, illustrating its molecular arrangement including a tropane ring, ester linkage, phenyl group, and sulfate and water components.*
FDA Label Image

1 (Atropine Sulfate Ophthalimic Solution 2)

1 (Atropine Sulfate Ophthalimic Solution 2)
Label for Atropine Sulfate Ophthalmic Solution, USP 1%, 10 mg/mL, 2 mL sterile eye drops. The label includes dosage form and strength, usage for topical application to the eye, active ingredient amount, preservative details, storage instructions (20° to 25°C), warning to keep out of reach of children, and distributor Amneal Pharmaceuticals LLC. Barcode and manufacturing details are also shown.*
FDA Label Image

1 (Atropine Sulfate Ophthalimic Solution 3)

1 (Atropine Sulfate Ophthalimic Solution 3)
Atropine Sulfate Ophthalmic Solution USP 1%, 2 mL carton label by Amneal Pharmaceuticals NY LLC. The label states the product is sterile and for topical application to the eye, listing atropine sulfate 10 mg/mL (1%) as active ingredient. Inactive ingredients and storage instructions are included. The label also has a warning to keep out of reach of children, manufacturing and distribution details, and a barcode.*
FDA Label Image

1 (Atropine Sulfate Ophthalimic Solution 4)

1 (Atropine Sulfate Ophthalimic Solution 4)
Label for Atropine Sulfate Ophthalmic Solution USP 1%, 5 mL sterile drops. Contains atropine sulfate 10 mg/mL and benzalkonium chloride preservative. Distributed by Amneal Pharmaceuticals LLC. Includes storage instructions and a warning to keep out of reach of children.*
FDA Label Image

1 (Atropine Sulfate Ophthalimic Solution 5)

1 (Atropine Sulfate Ophthalimic Solution 5)
Atropine Sulfate Ophthalmic Solution, USP 1%, 10 mg/mL, 5 mL, sterile solution for topical eye application. The label shows the active ingredient as atropine sulfate and lists inactives including benzalkonium chloride. Manufactured by Amneal Pharmaceuticals Pvt. Ltd. and distributed by Amneal Pharmaceuticals LLC. The package includes storage instructions and a warning to keep out of reach of children.*
FDA Label Image

1 (Atropine Sulfate Ophthalimic Solution 6)

1 (Atropine Sulfate Ophthalimic Solution 6)
Atropine Sulfate Ophthalmic Solution USP 1%, a sterile eye drop solution for topical application to the eye. The label indicates a 15 mL bottle size. The active ingredient concentration is 10 mg/mL. Manufactured by Amneal Pharmaceuticals LLC, the label includes dosage, storage instructions, and a warning to keep out of reach of children, along with a barcode.*
FDA Label Image

1 (Atropine Sulfate Ophthalimic Solution 7)

1 (Atropine Sulfate Ophthalimic Solution 7)
Atropine Sulfate Ophthalmic Solution, USP 1%, 15 mL carton label by Amneal Pharmaceuticals NY LLC. The label indicates a sterile solution for topical application to the eye, with atropine sulfate USP 10 mg/mL as the active ingredient. It includes inactive ingredients, storage instructions, a warning to keep out of reach of children, and manufacturer and distributor information for Amneal Pharmaceuticals Pvt. Ltd. and Amneal Pharmaceuticals LLC.*

* 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.