---
brand_name: "DURICEF"
generic_name: "CEFADROXIL/CEFADROXIL HEMIHYDRATE"
slug: "cefadroxil-cefadroxil-hemihydrate"
canonical_url: "https://medichelpline.com/drug-index/cefadroxil-cefadroxil-hemihydrate"
content_type: "drug_monograph"
route: "ORAL"
drug_class: "General Medications"
fda_updated_at: "2007-06-05T00:00:00.000Z"
license: "Drugs@FDA Public Domain / Informational Use"
---
# DURICEF (CEFADROXIL/CEFADROXIL HEMIHYDRATE)
## Clinical Monograph Metadata
- **Canonical URL:** https://medichelpline.com/drug-index/cefadroxil-cefadroxil-hemihydrate
- **Generic / Active Ingredient:** CEFADROXIL/CEFADROXIL HEMIHYDRATE
- **Brand Name:** DURICEF
- **Administration Route:** ORAL
- **Pharmacological Class:** General Medications
- **FDA Data Timestamp:** 2007-06-05T00:00:00.000Z
## Primary Indication & Clinical Use
Please see www.fda.gov/STIC for labeling requirements on susceptibility test interpretive criteria for systemic antibacterial and antifungal drugs. Review priority: STANDARD Marketing status: Discontinued
## Monograph Summary

Approval overview DURICEF is listed in Drugs@FDA under application 050512 (NDA). Please see www.fda.gov/STIC for labeling requirements on susceptibility test interpretive criteria for systemic antibacterial and antifungal drugs. Review priority: STANDARD Marketing status: Discontinued Active ingredient CEFADROXIL/CEFADROXIL HEMIHYDRATE Form and strength CAPSULE;ORAL - EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor WARNER CHILCOTT Submission history Latest submission status date: 2007-06-05 00:00:00. Submission type: SUPPL.

## Primary Sources & FDA Regulatory Records
- [Drugs@FDA Primary Database](https://www.accessdata.fda.gov/scripts/cder/daf/) (Reference Slug: `cefadroxil-cefadroxil-hemihydrate`)
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