# Amoxicillin

NDC: 65862-070
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: 20061228

FDA application: ANDA065334

## Active ingredients

- AMOXICILLIN: 200 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65862-070"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65862-070
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3cacd754-73f4-496e-a529-9ca39fa6692d