# Fosinopril sodium

NDC: 76282-201
Generic name: Fosinopril sodium
Labeler / Manufacturer: Exelan Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20050621

FDA application: ANDA077222

## Active ingredients

- FOSINOPRIL SODIUM: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"76282-201"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76282-201
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e2ff3171-a17a-456a-9272-ca1682b01d19