# Nortriptyline Hydrochloride

NDC: 51672-4002
Generic name: Nortriptyline Hydrochloride
Labeler / Manufacturer: Taro Pharmaceuticals U.S.A., Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20000508

FDA application: ANDA075520

## Active ingredients

- NORTRIPTYLINE HYDROCHLORIDE: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-4002"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-4002
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=aee2c1a1-d848-4c3b-8c6d-8a4f6ce94c28