# Amoxicillin

NDC: 0143-9889
Generic name: Amoxicillin
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: 20060619

FDA application: ANDA065322

## Active ingredients

- AMOXICILLIN: 250 mg/5mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0143-9889"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0143-9889
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=077f4a65-3cfb-4cb1-99f2-e27ffc5939c0