# Protriptyline Hydrochloride

NDC: 42794-007
Generic name: Protriptyline Hydrochloride
Labeler / Manufacturer: Sigmapharm Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200302

FDA application: ANDA090462

## Active ingredients

- PROTRIPTYLINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42794-007"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42794-007
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a023e637-bee9-8c86-e053-2a95a90aa488