# Ampicillin

NDC: 65219-014
Generic name: ampicillin sodium
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20191030

FDA application: ANDA062719

## Active ingredients

- AMPICILLIN SODIUM: 250 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65219-014"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65219-014
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8dbb4c71-8543-08f1-e053-2995a90af88d