Prednisolone Acetate Suspension/ Drops
Product Images NDC 60219-2552

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Prednisolone Acetate (NDC 60219-2552). 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

1 (Prednisolone Acetate Ophthalmic Suspension 1)

Chemical structure of prednisolone acetate showing its steroid backbone with hydroxyl and acetoxy functional groups.*

FDA Label Image

1 (Prednisolone Acetate Ophthalmic Suspension 2)

The label for Prednisolone Acetate Ophthalmic Suspension, USP 1%, 5 mL sterile drops, highlights its use for the eye only. The label includes active ingredient prednisolone acetate at 10 mg/mL, preservative benzalkonium chloride, dosage instructions to shake well before use, and storage conditions between 2°C to 30°C. Manufactured and distributed by Amneal Pharmaceuticals NY LLC, with a barcode and space for batch lot and expiration date printing.*

FDA Label Image

2 (Prednisolone Acetate Ophthalmic Suspension 3)

Packaging label for prednisoLONE Acetate Ophthalmic Suspension, USP 1% by Amneal Pharmaceuticals NY LLC. This sterile eye drop suspension is presented in a 5 mL container. The label includes product concentration, directions for use, storage instructions, and barcodes, along with manufacturer and distributor information.*

FDA Label Image

3 (Prednisolone Acetate Ophthalmic Suspension 4)

Label for prednisoLONE Acetate Ophthalmic Suspension, USP 1% (prednisolone acetate) sterile eye drops in a 10 mL bottle. The label includes active ingredient and preservative information, usage instructions emphasizing eye use only, storage guidelines, and manufacturer details (Amneal Pharmaceuticals LLC). It features a barcode and space for batch and expiration dates.*

FDA Label Image

4 (Prednisolone Acetate Ophthalmic Suspension 5)

Packaging label for prednisoLONE Acetate Ophthalmic Suspension, USP 1% by Amneal Pharmaceuticals NY LLC. The label indicates it is a sterile ophthalmic suspension for eye use only, in a 10 mL bottle filled to two-thirds capacity. The product contains prednisolone acetate 1% with benzalkonium chloride as a preservative, and storage instructions are provided. Manufactured by Amneal Pharmaceuticals Pvt. Ltd., India, and distributed by Amneal Pharmaceuticals LLC, NJ.*

FDA Label Image

4 (Prednisolone Acetate Ophthalmic Suspension 6)

Label for prednisolone acetate 1% ophthalmic suspension, USP, 15 mL sterile bottle. The label includes the product name prednisoLONE Acetate Ophthalmic Suspension, 1%, with active ingredient prednisolone acetate and preservative benzalkonium chloride. It specifies the use as 'FOR EYE USE ONLY' and includes storage instructions and manufacturer information for Amneal Pharmaceuticals NY LLC. The label shows the NDC 60219-2552-1 and indicates it is a prescription-only product.*

FDA Label Image

6 (Prednisolone Acetate Ophthalmic Suspension 7)

Packaging label for prednisoLONE Acetate Ophthalmic Suspension, USP 1%, a 15 mL sterile eye drop suspension by Amneal Pharmaceuticals NY LLC. The label includes active ingredient prednisolone acetate 1%, warnings for eye use only, storage instructions, and manufacturer information for Amneal Pharmaceuticals Pvt. Ltd. in India and distributor details in New Jersey, USA.*

* 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.