# Felodipine

NDC: 0603-3583
Generic name: Felodipine
Labeler / Manufacturer: Endo USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20111215

FDA application: ANDA200815

## Active ingredients

- FELODIPINE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0603-3583"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0603-3583
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=55637724-8757-11de-8a39-0800200c9a66