Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

PrediniSONE Tablets Recalled by Par Pharmaceutical Inc. Due to Labeling: Incorrect or Missing Exp Date - An...

Date: March 4, 2020
Company: Par Pharmaceutical Inc.
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Par Pharmaceutical Inc. directly.

Affected Products

PrediniSONE Tablets, USP 5 mg, 48-count bottle, Rx only, Distributed by: Par Pharmaceutical Chestnut Ridge, NY 10977, NDC 0603-5337-31

Quantity: 13008 bottles

Why Was This Recalled?

Labeling: Incorrect or Missing Exp Date - An incorrect expiration date has been identified on Prednisone Tablets USP 5 mg

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Par Pharmaceutical Inc.

Par Pharmaceutical Inc. has 8 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report