# Sildenafil Citrate

NDC: 70771-1668
Generic name: Sildenafil Citrate
Labeler / Manufacturer: Zydus Lifesciences Limited
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

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70771-1668"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70771-1668
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2ef4d02f-76ee-4f67-9f4f-1cd554decb31