Drug recalls

Atomoxetine Capsules, USP, 18 mg, 30 capsule bottles, Rx Only, Manufactured for: Northstar Rx LLC., Memphis, TN 38141, Manufactured by: Gle…

Glenmark Pharmaceuticals Inc., USA · CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.

Class IIOngoingD-0239-2025
Status
Ongoing
City
Mahwah
State
NJ
Country
United States
Classification
Class II
Product type
Drugs
Event ID
96194
Recalling firm
Glenmark Pharmaceuticals Inc., USA
Address 1
750 Corporate Dr
Address 2
N/A
Postal code
07430-2009
Voluntary mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Distribution pattern
Nationwide within the U.S
Recall number
D-0239-2025
Product quantity
119,040 bottles
Reason for recall
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.
Recall initiation date
20250129
Center classification date
20250220
Report date
20250226
Product description

Atomoxetine Capsules, USP, 18 mg, 30 capsule bottles, Rx Only, Manufactured for: Northstar Rx LLC., Memphis, TN 38141, Manufactured by: Glenmark Pharmaceuticals Ltd., Goa, India, NDC 16714-756-01.

Code info

Lot Numbers: 19233228, 19233227, Exp.: 7/2025; 19233757, Exp.: 8/2025; 19234229, Exp.: 9/2025; 19235090, Exp.: 11/2025; 19241471, Exp.:3/2026; 19242180, Exp.: 5/2026.

Harmonized identifiers (openFDA)
Application number
ANDA079019
Brand name
ATOMOXETINE
Generic name
ATOMOXETINE
Manufacturer name
Northstar Rx LLC
Product NDC
16714-755, 16714-756, 16714-757, 16714-758, 16714-759, 16714-760, 16714-761
Product type
HUMAN PRESCRIPTION DRUG
Route
ORAL
Substance name
ATOMOXETINE HYDROCHLORIDE
RxCUI
349591, 349592, 349593, 349594, 349595, 608139, 608143
SPL ID
a0f55e56-0899-430c-b25d-475d713f3a93
SPL set ID
133a4b65-762b-4712-baba-2442546f0379
Package NDC
16714-755-01, 16714-756-01, 16714-757-01, 16714-758-01, 16714-759-01, 16714-760-01, 16714-761-01
Is original packager
true
Upc
0316714760018, 0316714755014, 0316714756011, 0316714761015, 0316714757018
UNII
57WVB6I2W0
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.