# Cefadroxil

NDC: 16714-389
Generic name: Cefadroxil
Labeler / Manufacturer: NorthStar Rx LLC
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: 250 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16714-389"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16714-389
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=30bb3686-87b4-4676-9ff5-e20deb8bff9d