# Imipramine hydrochloride

NDC: 80425-0294
Generic name: Imipramine hydrochloride
Labeler / Manufacturer: Advanced Rx Pharmacy of Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230404

FDA application: ANDA040903

## Active ingredients

- IMIPRAMINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80425-0294"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0294
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f887062a-7c82-664f-e053-6294a90a2773