# Augmentin

NDC: 71297-240
Generic name: Amoxicillin and Clavulanate Potassium
Labeler / Manufacturer: Allegis Holdings, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: FOR SUSPENSION
Routes: ORAL
Marketing started: 20230901

FDA application: NDA050575

## Active ingredients

- AMOXICILLIN: 125 mg/5mL
- CLAVULANATE POTASSIUM: 31.25 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71297-240"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71297-240
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=04a31a42-d79e-bbb4-e063-6394a90a63ee