Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 68180-0492-01 recalled?

Clomipramine Hydrochloride · 100 CAPSULE in 1 BOTTLE (68180-492-01)

Yes — this exact package was recalled

2 FDA recalls name the code 68180-0492-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

Active ingredient
Clomipramine Hydrochloride Capsules
Strength
CLOMIPRAMINE HYDROCHLORIDE 25 mg/1
Form
Capsule · Oral
Labeler
Lupin Pharmaceuticals, Inc.
Type
Human Prescription Drug
Product code
68180-0492

Recalls naming this package

Class II · Moderate risk

clomiPRAMINE Hydrochloride Capsules USP 25 mg

Failed Impurities/Degradation Specifications: an out of specification result observed in degradation product test (any unspecified degradation product) during retention sample testing at expiry.

Terminated Impurity / degradation Lupin Pharmaceuticals Inc. NDC 68180-492-01 D-0537-2025
Class II · Moderate risk

clomiPRAMINE hydrochloride Capsules USP

Failed Impurities/Degradation Specifications: an out of specification result observed in degradation product test (any unspecified degradation product) during 18-month long term stability study.

Terminated Impurity / degradation Lupin Pharmaceuticals Inc. NDC 68180-492-01 D-0377-2025

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.

Other recalled products from this labeler