Atropine Solution/ Drops
Product Images NDC 68083-669

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 68083-669). 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

Atropine-sulfate-oph-spl-carton-15ml (Atropine Sulfate Oph Spl Carton 15ml)

Atropine-sulfate-oph-spl-carton-15ml (Atropine Sulfate Oph Spl Carton 15ml)
Atropine Sulfate Ophthalmic Solution, USP 1% 15 mL bottle carton label. The label shows it is a sterile ophthalmic solution for eye use only with a 10 mg/mL strength. It is manufactured by Gland Pharma Limited, Hyderabad, India. The label includes storage instructions, ingredient details, Rx only designation, and a barcode. An eye image is also present on the label.*
FDA Label Image

Atropine-sulfate-oph-spl-carton-2ml (Atropine Sulfate Oph Spl Carton 2ml)

Atropine-sulfate-oph-spl-carton-2ml (Atropine Sulfate Oph Spl Carton 2ml)
Packaging label for Atropine Sulfate Ophthalmic Solution, USP 1% by Gland Pharma Limited. The 2 mL sterile solution has an active strength of 10 mg/mL (1%) atropine sulfate, intended for eye use only. The label includes storage instructions, a barcode, and manufacturer information from Hyderabad, India.*
FDA Label Image

Atropine-sulfate-oph-spl-carton-5ml (Atropine Sulfate Oph Spl Carton 5ml)

Atropine-sulfate-oph-spl-carton-5ml (Atropine Sulfate Oph Spl Carton 5ml)
Packaging label for Atropine Sulfate Ophthalmic Solution, USP 1%, 5 mL, by Gland Pharma Limited. The label indicates Rx only status, sterile ophthalmic solution use, and lists active and inactive ingredients including Atropine Sulfate 10 mg/mL. Storage and warning instructions are provided along with manufacturer details and a barcode.*
FDA Label Image

Atropine-sulfate-oph-spl-label-15ml (Atropine Sulfate Oph Spl Label 15ml)

Atropine-sulfate-oph-spl-label-15ml (Atropine Sulfate Oph Spl Label 15ml)
Atropine Sulfate Ophthalmic Solution USP 1%, 15 mL bottle label by Gland Pharma Limited. It includes the active ingredient Atropine Sulfate 10 mg/mL and a preservative Benzalkonium Chloride 0.1 mg/mL. The label also notes the product is sterile, for eye use only, Rx only, with storage instructions and a warning to keep out of reach of children.*
FDA Label Image

Atropine-sulfate-oph-spl-label-2ml (Atropine Sulfate Oph Spl Label 2ml)

Atropine-sulfate-oph-spl-label-2ml (Atropine Sulfate Oph Spl Label 2ml)
Atropine Sulfate Ophthalmic Solution USP 1%, 2 mL bottle label from Gland Pharma Limited. The label indicates the product is sterile and intended for ophthalmic use. It lists the active ingredient concentration as atropine sulfate 10 mg/mL (1%) and includes storage and safety warnings. The label includes a barcode and manufacturing details from Gland Pharma Limited in Hyderabad, India.*
FDA Label Image

Atropine-sulfate-oph-spl-label-5ml (Atropine Sulfate Oph Spl Label 5ml)

Atropine-sulfate-oph-spl-label-5ml (Atropine Sulfate Oph Spl Label 5ml)
Label for Atropine Sulfate Ophthalmic Solution USP 1%, 5 mL, manufactured by Gland Pharma Limited. The label indicates it is a sterile ophthalmic solution for eye use only, containing 10 mg/mL atropine sulfate. It includes storage instructions, preservative information, warnings, a barcode, lot and expiration date fields, and manufacturing address details.*
FDA Label Image

Atropine-sulfate-oph-spl-str (Atropine Sulfate Oph Spl Str)

Atropine-sulfate-oph-spl-str (Atropine Sulfate Oph Spl Str)
Chemical structure diagram of Atropine Sulfate, showing the molecular composition including functional groups and sulfate and water molecules.*

* 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.