# Amoxicillin and Clavulanate Potassium

NDC: 0093-2277
Generic name: Amoxicillin and Clavulanate Potassium
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20050113

FDA application: ANDA065089

## Active ingredients

- AMOXICILLIN: 200 mg/5mL
- CLAVULANATE POTASSIUM: 28.5 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0093-2277"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-2277
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=963e7bea-ff5d-420a-9cb2-e4aefb534b33