# Imipramine Hydrochloride

NDC: 70868-810
Generic name: Imipramine Hydrochloride
Labeler / Manufacturer: Key Therapeutics
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220718

FDA application: ANDA040751

## Active ingredients

- IMIPRAMINE HYDROCHLORIDE: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70868-810"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70868-810
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9c685c94-64cd-442a-ade7-193c62d7a058