# SILDENAFIL CITRATE

NDC: 60290-002
Generic name: SILDENAFIL CITRATE
Labeler / Manufacturer: Umedica Laboratories USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260215

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:"60290-002"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60290-002
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=90477a51-63ba-43f4-a74b-4659a946093c