# Amoxicillin and Clavulanate Potassium

NDC: 70882-111
Generic name: Amoxicillin and Clavulanate Potassium
Labeler / Manufacturer: Cambridge Therapeutics Technologies, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20050823

FDA application: ANDA065189

## Active ingredients

- AMOXICILLIN: 250 mg/1
- CLAVULANATE POTASSIUM: 125 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70882-111"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70882-111
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a4c9694c-f539-470e-bfe3-8723fa1c343d