Product Recalls & Refunds Online / National

Asclemed USA Inc.: Duloxetine DR Capsules, 30 mg, 30 count bottles, Rx, Relabeled by: Enovachem Pharmaceuticals, Torrance, CA 90501, NDC 76420-634-30, Marketed by: Ajanta Pharma USA Inc.

Reward FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price

Recall reason: CGMP Deviations; presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the FDA acceptable intake limit.. Recalled by Asclemed USA Inc.. Distribution: US Nationwide.. Classification (Class II — potential health risk). Affected lots/NDC/dates: Lot # 050725G-30 & 050725F-30, Exp Date: 06/30/2026. Return the recalled medication to the pharmacy where you purchased it for a full refund of the purchase price.

Reward FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price

Category Product Recalls & Refunds

Location National

Eligibility U.S. consumers who purchased the recalled drug or medication. Return it to the pharmacy where you bought it for a full refund. You generally do not need the original receipt — the pharmacist can look up your purchase history.

Source Official Source ↗

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