# Cefadroxil

NDC: 57237-098
Generic name: Cefadroxil
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20130425

FDA application: ANDA065349

## Active ingredients

- CEFADROXIL: 500 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"57237-098"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57237-098
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6e4111d3-f11b-403c-b340-b216022709df