# Amoxicillin

NDC: 60687-809
Generic name: Amoxicillin
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250325
Marketing ended: 20261231
FDA application: ANDA065256

## Active ingredients

- AMOXICILLIN: 875 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60687-809"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-809
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d339ea0f-8797-460f-a3b7-b8455c250366