# SILDENAFIL CITRATE

NDC: 71205-721
Generic name: SILDENAFIL CITRATE
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200904

FDA application: ANDA209302

## Active ingredients

- SILDENAFIL CITRATE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71205-721"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-721
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=59b623bc-fbdd-4f32-8327-0d600763f429