US Drug Recall Register
Class II · Moderate risk Terminated Initiated Oct 25, 2019 (7 years ago)

Novitium Pharma Ranitidine Capsules 300 mg 30 capsules Rx Only Manufactured by: Novitium…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP Deviations: Presence of NDMA impurity detected in product.

What was recalled

Novitium Pharma Ranitidine Capsules 300 mg 30 capsules Rx Only Manufactured by: Novitium Pharma LLC 70 Lake Drive, East Windsor, New Jersey 08520 NDC 70954-002-10

Recalling firm
Novitium Pharma LLC
NDC code
70954-002-10
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0312-2020

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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