# Amoxicillin

NDC: 65862-706
Generic name: Amoxicillin
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20140915

FDA application: ANDA204030

## Active ingredients

- AMOXICILLIN: 125 mg/5mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65862-706"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65862-706
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=234d0dfc-cb24-413f-b798-129c73eb848e