Product Images Prednisolone Acetate

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Product Label Images

The following 2 images provide visual information about the product associated with Prednisolone Acetate NDC 70518-4006 by Remedyrepack Inc., such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

Remedy_Label - Remedy Label

Remedy_Label - Remedy Label

This is a description of a medication labeled as "RX ONLY." The National Drug Code (NDC) is 70518-4006-00, with an expiration date and LOT# not specified. The source NDC is 61314-0637-05. The manufacturer is Sandoz Inc., located in Princeton, NJ 08540. The medication is prednisolone acetate 1% ophthalmic suspension, available in a quantity of 5 mL. It is intended for topical ophthalmic use and should be shaken well before use. The packaging is referred to as "Orépack." The directions for use are provided in the package insert. It should be stored between 20-25°C (58-77°F), with excursions permitted up to 15-30°C (59-86°F) as allowed by USP guidelines. The medication has been repackaged by RemedyRepack Inc., located in Indiana, PA 15701, with contact information provided as 724.465.8762.*

chemical - chemical

chemical - chemical

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.