# Selegiline Hydrochloride

NDC: 72319-006
Generic name: Selegiline Hydrochloride
Labeler / Manufacturer: i3 Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20211215

FDA application: ANDA074672

## Active ingredients

- SELEGILINE HYDROCHLORIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72319-006"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72319-006
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c81e983b-455d-2e65-e053-2a95a90a3123