# Sildenafil

NDC: 72865-105
Generic name: Sildenafil
Labeler / Manufacturer: XLCare Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20190710

FDA application: ANDA203623

## Active ingredients

- SILDENAFIL CITRATE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72865-105"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72865-105
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=22d70b8d-41bc-416d-89e9-e4c39db0af83