# Imipramine Hydrochloride

NDC: 69315-134
Generic name: Imipramine Hydrochloride
Labeler / Manufacturer: Leading Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20160407

FDA application: ANDA040903

## 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:"69315-134"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69315-134
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=490263ce-b4d2-428a-87da-fcd07f85499a