# SILDENAFIL CITRATE

NDC: 71335-3111
Generic name: SILDENAFIL
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20180611

FDA application: ANDA091448

## 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:"71335-3111"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-3111
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a05ab4e7-6f70-41c3-a3b7-9a2fd7a1d2d6