# Sildenafil Citrate

NDC: 70710-1716
Generic name: Sildenafil Citrate
Labeler / Manufacturer: Zydus Pharmaceuticals (USA) Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20221027

FDA application: ANDA215708

## Active ingredients

- SILDENAFIL CITRATE: 10 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70710-1716"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70710-1716
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b2f04ce4-f19c-403d-8a83-74f123e5d30a