# Sildenafil

NDC: 71205-088
Generic name: Sildenafil
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20171211

FDA application: ANDA077342

## Active ingredients

- SILDENAFIL CITRATE: 100 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71205-088"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-088
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=43a036a4-8a34-4411-ac8e-bf5063d67d48