# Selegiline Hydrochloride

NDC: 71205-888
Generic name: Selegiline Hydrochloride
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20190402

FDA application: ANDA206803

## 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:"71205-888"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-888
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=57b564ef-c89b-4cf6-a11f-f67391d74e7e
