NDC 69584-426

Imipramine Hydrochloride 25 mg tablet

On the label: Oxford Pharmaceuticals, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Oxford Pharmaceuticals, LLCBirmingham, AL, United StatesMakes it Problems found, fixed voluntarilyNov 3, 2023 · 3 inspections

Product details

Generic drug
Imipramine: every company that makes it
Form
tablet, oral
Strength
25 mg
Approval
ANDA ANDA040751
On the market since
Aug 1, 2020
Package NDCs
69584-426-10 69584-426-90
Official label
DailyMed (National Library of Medicine), updated Feb 17, 2026

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