Class III โ€” Low Risk

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

Digoxin Tablets Recalled by Novitium Pharma LLC Due to Cross Contamination with Other Products:(mycophenolate mofetil).

Date: March 4, 2024
Company: Novitium Pharma LLC
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 Novitium Pharma LLC directly.

Affected Products

Digoxin Tablets, USP 125mcg, (0.125 mg), 1000-count bottle, Rx Only, Manufactured by: Novitium Pharma LLC., 70 Lake Drive, East Windsor, New Jersey 08520, NDC 70954-201-20

Quantity: 3,940 1000-count bottles

Why Was This Recalled?

Cross Contamination with Other Products:(mycophenolate mofetil).

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Novitium Pharma LLC

Novitium Pharma LLC has 6 total recalls tracked by RecallDetector.

Related Recalls

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