# NORTRIPTYLINE HYDROCHLORIDE

NDC: 61919-353
Generic name: NORTRIPTYLINE HYDROCHLORIDE
Labeler / Manufacturer: DIRECT RX
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20210915

FDA application: ANDA075520

## Active ingredients

- NORTRIPTYLINE HYDROCHLORIDE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"61919-353"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=61919-353
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=45884cad-4a2d-44f4-93bd-16b130daf32d