# Nortriptyline Hydrochloride

NDC: 0093-0812
Generic name: Nortriptyline Hydrochloride
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 19950405

FDA application: ANDA074132

## Active ingredients

- NORTRIPTYLINE HYDROCHLORIDE: 50 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0093-0812"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-0812
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b58d473a-b19f-4d2a-b1ae-dd398d7a29e1