# Clomipramine Hydrochloride

NDC: 69315-166
Generic name: Clomipramine Hydrochloride
Labeler / Manufacturer: Leading Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20200310

FDA application: ANDA211364

## Active ingredients

- CLOMIPRAMINE HYDROCHLORIDE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69315-166"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69315-166
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fa0d4de8-c96e-429d-a65c-928afbf46863