FDA recall record

Atomoxetine Capsules, USP, 80 mg, 30 capsule bottles recall — FDA D-0243-2025

CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.

Class IIclassification
D-0243-2025official record ID
Feb 26, 2025report date

Recall record at a glance

Official recordD-0243-2025
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmGlenmark Pharmaceuticals Inc., USA
Report dateFeb 26, 2025
Recall initiation dateJan 29, 2025
Quantity58,416 bottles
LocationMahwah, NJ, United States

Official product description

Atomoxetine Capsules, USP, 80 mg, 30 capsule bottles, Rx Only, Manufactured for: Northstar Rx LLC., Memphis, TN 38141, Manufactured by: Glenmark Pharmaceuticals Ltd., Goa, India, NDC 16714-760-01.

Why the product was recalled

CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.

Distribution information

Nationwide within the U.S

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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