# CLOMIPRAMINE HYDROCHLORIDE

NDC: 51672-4013
Generic name: Clomipramine Hydrochloride
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 19961231

FDA application: ANDA074694

## Active ingredients

- CLOMIPRAMINE HYDROCHLORIDE: 75 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-4013"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-4013
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=db752dbd-be41-4cdd-8a13-ed1ff9ef7461