# AMPICILLIN

NDC: 0404-9818
Generic name: AMPICILLIN SODIUM
Labeler / Manufacturer: Henry Schein, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20220117

FDA application: ANDA065499

## Active ingredients

- AMPICILLIN SODIUM: 2 g/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0404-9818"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0404-9818
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=06ca924c-5f3a-4924-90f4-5ba623daaa0e