# escitalopram

NDC: 16571-756
Generic name: escitalopram
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230610

FDA application: ANDA078777

## Active ingredients

- ESCITALOPRAM OXALATE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16571-756"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16571-756
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ccbe97b5-da68-4fff-929a-240dd705fe6f