# Amoxicillin and Clavulanate Potassium

NDC: 0143-9982
Generic name: Amoxicillin and Clavulanate Potassium
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20071201

FDA application: ANDA065191

## Active ingredients

- AMOXICILLIN: 400 mg/5mL
- CLAVULANIC ACID: 57 mg/5mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0143-9982"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0143-9982
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=240bcdcb-31d9-40a0-87e1-bd16264a2e20