Published recall report · ImpurityUpdated · 1 yr 6 mo ago
Rising Pharma Holding, Inc. recall: Duloxetine Delayed-Release Capsules, USP, 30 mg, 1,000-count bottle, Rx only, Distributed by: Rising Health, LLC, Saddle Brook, NJ 07663, NDC 57237-018-99
Duloxetine Delayed-Release Capsules, USP, 30 mg, 1,000-count bottle, Rx only, Distributed by: Rising Health, LLC, Saddle Brook, NJ 07663, NDC 57237-018-99
Current recall status is unverified. FDA does not update drug-enforcement status after publication. Check the latest official information or ask a pharmacist.
What to do
Check the lot number on your pack against this recall and follow the firm's instructions. Do not stop taking a prescribed medicine without talking to a pharmacist or doctor first.
FDA public enforcement report, opens in a new tabWhich products
Duloxetine Delayed-Release Capsules, USP, 30 mg, 1,000-count bottle, Rx only, Distributed by: Rising Health, LLC, Saddle Brook, NJ 07663, NDC 57237-018-99
- Producer
- Rising Pharma Holding, Inc.
DTB23111A
- Dates on pack
- Lot #: DTB23111A, Exp 8/31/2025
More detail
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended interim limit.
In the news
Reporting from news publishers. Follow the official notice for product advice.
No news stories about this recall yet.