NDC 69315-135

Imipramine Hydrochloride 50 mg tablet, film coated

On the label: Leading Pharma, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Leading Pharma, LLCFairfield, NJ, United StatesMakes it Problems found, fixed voluntarilyOct 21, 2024 · 13 inspections

Product details

Generic drug
Imipramine: every company that makes it
Form
tablet, film coated, oral
Strength
50 mg
Approval
ANDA ANDA040903
On the market since
Apr 7, 2016
Package NDCs
69315-135-01 69315-135-10
Official label
DailyMed (National Library of Medicine), updated Aug 11, 2026

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