# Sildenafil Citrate

NDC: 67877-648
Generic name: Sildenafil Citrate
Labeler / Manufacturer: Ascend Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20191129

FDA application: ANDA212440

## Active ingredients

- SILDENAFIL CITRATE: 10 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67877-648"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67877-648
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a0fa4162-e1b7-4293-ab7d-c5b375779060