# Nortriptyline Hydrochloride

NDC: 67046-1500
Generic name: Nortriptyline Hydrochloride
Labeler / Manufacturer: Coupler LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20250128

FDA application: ANDA073556

## Active ingredients

- NORTRIPTYLINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67046-1500"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67046-1500
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2ccb3fd0-53c9-6015-e063-6294a90a3fd6