# SILDENAFIL CITRATE

NDC: 72603-883
Generic name: SILDENAFIL CITRATE
Labeler / Manufacturer: Northstar Rx LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260224

FDA application: ANDA209302

## Active ingredients

- SILDENAFIL CITRATE: 25 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72603-883"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72603-883
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8127ff38-2761-49ec-8ce7-7f971f521cfb