# Amoxicillin

NDC: 43063-885
Generic name: Amoxicillin
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20060329

FDA application: ANDA065255

## 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:"43063-885"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43063-885
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=05b9b595-05d9-469f-82a3-c2bc94c50be2