# Amoxicillin

NDC: 0781-2613
Generic name: Amoxicillin
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 19940930

FDA application: ANDA064076

## Active ingredients

- AMOXICILLIN: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-2613"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-2613
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=13bd4214-9b7f-425b-af5f-fc1ddc678230