# Sildenafil

NDC: 72303-0847
Generic name: Sildenafil
Labeler / Manufacturer: HEC Pharm USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200611

FDA application: ANDA213032

## Active ingredients

- SILDENAFIL CITRATE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72303-0847"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72303-0847
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4c57d855-3b49-fe6e-e063-6294a90a5cd5