Pred-gati
Product Images NDC 70261-502

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Pred-gati (NDC 70261-502). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Imprimisrx Nj, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

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FDA Label Image

Bottle Label (Pg)

Bottle Label (Pg)
This is a description of an ophthalmic suspension medication compounded for a licensed professional or patient use. The medication contains Prednisolone-Gatifloxacin 1%/0.5%, Edetate Disodium, Sodium Phosphate Monobasic, Sodium Phosphate Dibasic Heptahydrate, Benzalkonium Chloride 50% and Sterile Water. The pH is adjusted using either Sodium Hydroxide or Hydrochloric Acid. This medication comes in a sterile 3.5 ml Bottle with NDC 70261-502-03 and should be stored at controlled room temperature. The prescription is for single-use only and should not be resold. The medication was compounded on 1705 Route 46 West, Suite 4, Lot # XXXXXXXXXXX, in Ledgewood, NJ 07852. The use-by date is not specified in the given text.*

* 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.