# Nortriptyline Hydrochloride

NDC: 70710-1156
Generic name: Nortriptyline Hydrochloride
Labeler / Manufacturer: Zydus Pharmaceuticals (USA) Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20220210

FDA application: ANDA213441

## Active ingredients

- NORTRIPTYLINE HYDROCHLORIDE: 75 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70710-1156"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70710-1156
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dbe85bdc-17a1-4201-bf48-a52e35d69b68