Prednisolone Acetate Suspension/ Drops
Product Images NDC 67296-2176

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Prednisolone Acetate (NDC 67296-2176). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Structure (F91d91ab 9100 4c26 967b 7d7efc290dc9 01)

FDA Label Image

Ndc 70748-332-02rx Onlyprednisolone Acetate Ophthalmic Suspension, Usp 1%sterile5 mL (F91d91ab 9100 4c26 967b 7d7efc290dc9 02)

Ndc 70748-332-02rx Onlyprednisolone Acetate Ophthalmic Suspension, Usp 1%sterile5 mL (F91d91ab 9100 4c26 967b 7d7efc290dc9 02)
Description: The text appears to be a label of a medication bottle containing prednisolone acetate. It lists the active and inactive ingredients, preservative, storage instructions, dosage information, manufacturer details, and batch coding information. The medication is manufactured for Lupin Pharmaceuticals in the United States. It also mentions that the bottle is filled to half capacity. The usual dosage instructions are to refer to the package insert, and it advises to shake well before using and to store the medication at temperatures up to 25°C.*
FDA Label Image

Ndc 70748-332-03rx Onlyprednisolone Acetate Ophthalmic Suspension, Usp 1%sterile10 mL (F91d91ab 9100 4c26 967b 7d7efc290dc9 03)

Ndc 70748-332-03rx Onlyprednisolone Acetate Ophthalmic Suspension, Usp 1%sterile10 mL (F91d91ab 9100 4c26 967b 7d7efc290dc9 03)
This is a medication label for Prednisolone Acetate eye drops, containing 1% prednisolone acetate and benzalkonium chloride as preservative. The inactive ingredients include boric acid, edetate disodium, hypromellose, polysorbate 80, sodium bisulfite, and sodium chloride. The product should be shaken well before use and stored at temperatures up to 25°C (77°F) to protect from freezing. The manufacturer is Lupin Limited, and the product is distributed by Lupin Pharmaceuticals, Inc. in Naples, FL, United States. The label also indicates that the bottle is filled to 2/3 capacity and the details like batch coding are overprinted at the plant.*
FDA Label Image

Ndc 70748-332-04rx Onlyprednisolone Acetate Ophthalmic Suspension, Usp 1%sterile15 mL (F91d91ab 9100 4c26 967b 7d7efc290dc9 04)

Ndc 70748-332-04rx Onlyprednisolone Acetate Ophthalmic Suspension, Usp 1%sterile15 mL (F91d91ab 9100 4c26 967b 7d7efc290dc9 04)
This is a pharmaceutical product label containing information about the medication. It includes details such as the active ingredient (prechisolone acetate), preservatives, inactive ingredients, manufacturer (Lupin Pharmaceuticals), storage instructions, dosage information, and batch coding. The product is a 15mL ophthalmic solution. Users are advised to refer to the package insert for usual dosage and to shake well before use.*
FDA Label Image

Image (F91d91ab 9100 4c26 967b 7d7efc290dc9 35 1)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.