Drug recalls

Testosterone Gel 1%, 2.5 grams, 30 Unit-dose packets in a carton, Rx only, Distributed by: Strides Pharma Inc., East Brunswick, NJ, NDC 643…

Strides Pharma, Inc. · Presence of foreign substance: Presence of Benzene.

Class IICompletedD-0293-2025
Status
Completed
City
Chestnut Ridge
State
NY
Country
United States
Classification
Class II
Product type
Drugs
Event ID
96412
Recalling firm
Strides Pharma, Inc.
Address 1
1 Ram Ridge Rd
Address 2
N/A
Postal code
10977-6714
Voluntary mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Distribution pattern
Nationwide in the U.S
Recall number
D-0293-2025
Product description
Testosterone Gel 1%, 2.5 grams, 30 Unit-dose packets in a carton, Rx only, Distributed by: Strides Pharma Inc., East Brunswick, NJ, NDC 64380-151-02
Product quantity
195,952 Cartons; 30 sachets/Carton.
Reason for recall
Presence of foreign substance: Presence of Benzene.
Recall initiation date
20250305
Center classification date
20250325
Report date
20250402
Code info

Lot #: 5501127A, 5501236A, Exp Apr-25; 5501341A, Exp Jun-25; 5501406A, Exp Jul-25; 5501408A, Exp Aug-25; 5501516A, Exp Sep-25; 5501568A, Exp Oct-25; 5501829A, Exp Mar-26; 5502000A, Exp Jul-26; 5502004A, 5502005A, Exp Aug-26; 5502092A, Exp Oct-26; 5502217A, Exp Dec-26; 5502262A, Exp Jan-27

Harmonized identifiers (openFDA)
Application number
ANDA076744
Brand name
TESTOSTERONE
Generic name
TESTOSTERONE
Manufacturer name
Strides Pharma Science Limited
Product NDC
64380-151, 64380-152
Product type
HUMAN PRESCRIPTION DRUG
Route
TRANSDERMAL
Substance name
TESTOSTERONE
RxCUI
1597123, 1597129
SPL ID
6d50f17e-4607-458a-882b-620daa3b58a9
SPL set ID
ee54c393-bcfe-4a52-b7b3-1da8750f35d9
Package NDC
64380-152-01, 64380-152-02, 64380-151-01, 64380-151-02
Is original packager
true
Upc
0364380151012, 0364380152019
Nui
N0000175824, N0000000146, M0001109
Pharm class epc
Androgen [EPC]
Pharm class moa
Androgen Receptor Agonists [MoA]
Pharm class cs
Androstanes [CS]
UNII
3XMK78S47O
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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.