# Amoxicillin

NDC: 51655-156
Generic name: Amoxicillin
Labeler / Manufacturer: Northwind Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20141106
Marketing ended: 20261031
FDA application: ANDA065271

## Active ingredients

- AMOXICILLIN: 500 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51655-156"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-156
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=26114563-c719-46da-b976-3e4271533f28