NDC 70868-810

Imipramine Hydrochloride 25 mg tablet, film coated

On the label: Key Therapeutics.

Where it's made

This label doesn't name the factory that makes the drug. Companies aren't required to print it on the label. The manufacturer's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Key Therapeutics uses for other drugs.

Product details

Generic drug
Imipramine: see every company that makes it
Form
tablet, film coated, oral
Strength
25 mg
Approval
ANDA ANDA040751
On the market since
Jul 18, 2022
Package NDCs
70868-810-10
Official label
DailyMed (National Library of Medicine), updated Oct 9, 2024

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