FDA-Drug2024-05-15Class II
Duloxetine Delayed-Release Capsules, USP, 20 mg, , 500-count bottles, Rx Only, Mfr. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcelona), Spain, Dist. by: Breckenridge Pharmaceuticals, Inc., Berkeley Heights, NJ 07922, NDC 51991-746-05.
Breckenridge Pharmaceutical, Inc
Hazard
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
Sold states
US Nationwide.
Affected count
7,188/ 500 count bottles
Manufactured in
15 Massirio Dr Ste 201, N/A, Berlin, CT, United States
Products
Duloxetine Delayed-Release Capsules, USP, 20 mg, , 500-count bottles, Rx Only, Mfr. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcelona), Spain, Dist. by: Breckenridge Pharmaceuticals, Inc., Berkeley Heights, NJ 07922, NDC 51991-746-05.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0483-2024Don't want to check this manually?
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