# Ampicillin and Sulbactam

NDC: 0409-2689
Generic name: Ampicillin sodium and Sulbactam sodium
Labeler / Manufacturer: Hospira, Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20060725
Marketing ended: 20261031
FDA application: ANDA065310

## Active ingredients

- AMPICILLIN SODIUM: 1 g/1
- SULBACTAM SODIUM: .5 g/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0409-2689"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0409-2689
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dc374fa4-350b-425d-a7db-7099fdc64cf1